Pleiotropic roles of cold shock proteins with special emphasis on unexplored cold shock protein member of Plasmodium falciparum
Malaria Journal volume 19, Article number: 382 (2020)
The cold shock domain (CSD) forms the hallmark of the cold shock protein family that provides the characteristic feature of binding with nucleic acids. While much of the information is available on bacterial, plants and human cold shock proteins, their existence and functions in the malaria parasite remains undefined. In the present review, the available information on functions of well-characterized cold shock protein members in different organisms has been collected and an attempt was made to identify the presence and role of cold shock proteins in malaria parasite. A single Plasmodium falciparum cold shock protein (PfCoSP) was found in P. falciparum which is reported to be essential for parasite survival. Essentiality of PfCoSP underscores its importance in malaria parasite life cycle. In silico tools were used to predict the features of PfCoSP and to identify its homologues in bacteria, plants, humans, and other Plasmodium species. Modelled structures of PfCoSP and its homologues in Plasmodium species were compared with human cold shock protein ‘YBOX-1’ (Y-box binding protein 1) that provide important insights into their functioning. PfCoSP model was subjected to docking with B-form DNA and RNA to reveal a number of residues crucial for their interaction. Transcriptome analysis and motifs identified in PfCoSP implicate its role in controlling gene expression at gametocyte, ookinete and asexual blood stages of malaria parasite. Overall, this review emphasizes the functional diversity of the cold shock protein family by discussing their known roles in gene expression regulation, cold acclimation, developmental processes like flowering transition, and flower and seed development, and probable function in gametocytogenesis in case of malaria parasite. This enables readers to view the cold shock protein family comprehensively.
Every organism faces changing environmental conditions and has evolved cellular machinery for coping with stress and adapting to changing environments. Change in temperature is one of the most common stresses faced by all living organisms. To respond to harmful effects of temperature downshift, there exists a family of proteins called cold shock proteins that play a significant role in acclimation of cells to cold [1,2,3,4,5]. They help the cells to adapt and have pleiotropic functions inside the cell [6, 7]. Cold shock proteins are among the most evolutionarily conserved proteins and are characterized by the presence of one or more cold shock domains (CSDs). CSDs have nucleic acid binding properties that bestow these proteins with several functions, including regulation of transcription, translation and splicing [5, 8].
At low temperatures, cold shock proteins function as RNA chaperones by destabilizing secondary structures in target RNA. This enables the maintenance of single stranded state of target RNA to pursue efficient transcription and translation [4, 9]. Cold shock proteins prevent formation of hairpin structures in RNA and, therefore, act as transcription anti-terminators [10, 11].
Identification of cold shock proteins in bacteria
Cold shock proteins were initially found when a sudden drop in temperature (from 37 °C to 10 °C) caused a many-fold increase in the expression of a cold shock protein A (CspA) in Escherichia coli [12, 13]. Thereafter, cold shock proteins have been identified in several bacteria, including psychrophilic, mesophilic, thermophilic, and even hyperthermophilic bacteria [4, 13, 14]. Sequence analysis indicates that bacterial cold shock proteins are small proteins with a molecular mass of approximately 7.4 kDa  and comprise a typical CSD. They all have the ability to bind single-stranded RNA and DNA but no double-stranded DNA [9, 16,17,18,19]. This protein-nucleic acid interaction is mediated by the moderately well-conserved nucleic acid binding motifs RNP1 (K/R-G-F/Y-G/A-F-V/I-X-F/Y) and RNP2 (L/I-F/Y-V/I-G/K-N/G-L) [2, 20,21,22].
In Escherichia coli, several cold induced proteins are expressed that include these cold shock proteins apart from RNA helicase csdA , exoribonucleases PNPase and RNase R , initiation factors 2a and 2b, NusA and RecA . Later, it was found that Escherichia coli encodes 9 cold shock protein genes (CspA to CspI) that share 46–91% amino acid sequence similarity . Naming of cold shock proteins is done in similar fashion to other bacteria, however identical names do not necessarily share identical function and structure in different bacteria. Among all cold shock proteins, CspC is constitutively expressed  whereas CspA, CspB, CspE, CspG, and CspI are induced by cold shock [27,28,29,30,31]. In contrast CspD is induced by stationary phase growth and nutrient starvation [32, 33] and cspF and cspH expression are not linked with any particular growth condition and their functions are not known . CspC and CspE are known to regulate the expression of stress response proteins ‘RpoS’ and ‘UspA’  while CspD is implicated in persister cell formation, biofilm development and inhibits DNA replication [36, 37].
CspA is the major cold shock protein and the most prominent one in Escherichia coli . A report by Giuliodori et al. suggested that mRNA of CspA adopts different structures at low temperature which makes it less prone to degradation . As a result CspA mRNA is translated more efficiently upon temperature fluctuation than CspA mRNA at 37 °C . Likewise, ttcsp2 of thermophilic Thermus thermophilus was also reported to be cold induced protein that adopt more stable secondary structure in response to temperature drop . At 37 °C, the cspA mRNA is very unstable, and has a half-life of only 12 s. Upon cold stress, its stability is dramatically increased as its half-life is now more than 20 min . This transient stabilization of cspA mRNA on temperature drop implicates its significance in induction during cold shock .
Xia et al. suggested that the functions of the CspA family members overlap and can compensate for each other . The authors found that by deleting 4 cold shock protein genes (cspA, cspB, cspE, cspG) in E. coli, a cold-sensitive strain ‘BX04’ was obtained that was unable to form colonies at 15 °C . The cold sensitivity of this strain can be suppressed by overexpressing any of the E. coli cold shock protein genes, except cspD. Moreover, loss of one or two cold shock protein genes in E. coli increased the production of the remaining cold-induced cold shock protein genes. Similarly, in Bacillus subtilis, deletion of one or two cold shock protein genes boosted the expression of remaining cold shock proteins post-cold shock .
The three-dimensional structures of several bacterial cold shock proteins have been determined [44,45,46,47]. Some of these include CspA from the mesophilic bacterium Escherichia coli (EcCspA), cold shock protein from the thermophilic bacterium Bacillus caldolyticus (BcCsp) and cold shock protein from the hyperthermophilic bacterium Thermotoga maritima (TmCsp) [44,45,46,47]. Structural studies indicate that cold shock proteins belong to oligonucleotide/oligosaccharide-binding (OB)-fold family of proteins. OB-fold consists of 5 antiparallel beta strands that form a Greek-key beta-barrel. Knowledge of OB-folded nucleoprotein complexes was found to originate from the X-ray structures of telomere DNA-binding proteins [48,49,50]. Although structurally cold shock proteins are conserved, their thermo-stability differs [14, 51]. Cold shock protein of thermophilic Thermus aquaticus has a melting temperature of 76 °C and a rigid structure. On the contrary, CspA of the psychrotrophic Listeria monocytogenes has a melting temperature of 40 °C . This implicates that psychrophilic cold shock proteins require higher structural flexibility to bind nucleic acids upon cold shock .
Cold shock proteins in humans
The human genome encodes for about 8 members of cold shock genes namely YBX1, YBX2, YBX3, CARHSP1, CSDC2, CSDE1, LIN28A, and LIN28B . The best characterized members are denoted Y-box binding protein family. The prototypic member is Y-box binding protein-1 (YB-1), encoded by the gene YBX1. Two other members of Y-box binding protein family exist namely DNA binding protein A (DbpA) and C (DbpC) that are encoded by the genes YBX3 and YBX2, respectively . YB-1 was first named in 1988 to refer to transcription factors that interact with the Ybox motif in the promoter of the major histocompatibility complex class II genes . YB-1 has properties of a nucleic acid chaperone and binds with both DNA and RNA. By its nuclei acid binding ability, it is involved in several mRNA- and DNA-dependent processes, including mRNA splicing, mRNA translation, DNA replication and repair [54,55,56,57,58,59]. The protein functions as a positive transcription factor to upregulate several genes, including MDR1 (multi-drug resistance-1) . The MDR1 promoter activity is known to increase in response to various environmental stimuli, including anticancer agents and ultraviolet irradiation [60, 61]. YB-1 also increases resistance of cells to ionizing radiation and xenobiotics when involved in DNA repair in the nucleus [61, 62]. YB-1 nuclear localization is therefore considered an early marker of multidrug resistance of malignant cells [62,63,64].
Another important cold shock protein expressed in humans is calcium-regulated heat-stable protein 1 (CARHSP1); a 24 kDa protein also known as CRHSP-24. CARHSP1 binds to tumor necrosis factor (TNF) mRNA and play a role in its stabilization within P-bodies and exosomes . It is dephosphorylated by calcium/calmodulin regulated protein phosphatase calcineurin . CARHSP1 is a paralogue of another cold shock protein PIPPin whose expression is limited to brain cells [67, 68]. PIPPin is known to bind specifically to the 3′-UTR ends of both histone H1 and H3.3 mRNAs, encompassing the polyadenylation signal . Its role is implicated in the negative regulation of histone variant synthesis in the developing brain . PIPPin also interacts with other RNA binding proteins such as hnRNP A1, hnRNP K, and YB-1 .
A further member of human cold shock protein is known as Unr (upstream of N-ras). It was first described as upstream of N-ras and initially identified as a regulator of N-ras expression [70,71,72,73]. Later it was found that Unr encodes a protein that possesses 5 CSDs, and is mainly expressed in the cytoplasm [74, 75]. The gene was then renamed as CSD containing E1 (CSDE1). CSDE1 plays a key role in translational reprogramming by determining the fate of mRNAs by changing their stability and abundance . CSDE1 promotes and represses the translation of RNAs and also increases and decreases their abundance. Hence the role of CSDE1 is considered bidirectional .
The final members of cold shock protein family in humans are denoted LIN28A or LIN28B, two highly related RNA binding proteins and proto-oncogenes . The role of LIN28 is to regulate translation of mRNAs that control developmental timing, pluripotency and metabolism . Besides, LIN28 is responsible for the repression of the let-7 microRNA biogenesis which is required for normal development and maintainence of the pluripotent state of cells [79,80,81].
Cold shock proteins in plants
Cold shock proteins play pleiotropic functions in plants ranging from acquiring freezing tolerance to regulating embryo development, flowering time and fruit development . WCSP1 is the wheat cold shock protein that was the first functionally characterized plant cold shock protein . It possesses biochemical functions similar to bacterial cold shock proteins and is involved in cold adaptation. WCSP1 shows binding with both DNA and RNA and unwinds double-stranded nucleic acids in vitro and in vivo [83,84,85]. In response to cold stress, there is upregulation of WCSP1 mRNA and increased expression of the corresponding protein in crown tissue during prolonged cold acclimation . Radkova et al. serologically characterized the temporal and spatial distribution of the wheat CSD proteins with regard to plant development and cold adaptation . They identified 4 wheat cold shock protein genes through database analysis and classified into three classes based on their molecular masses and protein domain structures. Class I (20 kDa) and class II (23 kDa) wheat cold shock proteins were observed to accumulate in root and shoot meristematic tissues during vegetative growth. Protein expression of class I and class II wheat cold shock proteins remained high during flower and seed development. On the contrary, class III wheat cold shock protein (27 kDa) was detected only during seed development. In response to cold stress, wheat cold shock proteins accumulate in crown tissue which suggests their role in cold acclimation .
Arabidopsis thaliana has 4 cold shock proteins 1–4 (AtCSP1-CSP4), that possess an N-terminal CSD. They all show binding with RNA, single and double-stranded DNA, and are able to unwind nucleic acid duplex. AtCSP3 (At2 g17870) is the only cold shock protein that is reported to be essential for the acquisition of freezing tolerance in Arabidopsis . Overexpression of AtCSP3 confers freezing tolerance by regulating expression of stress-related genes whose roles in freezing tolerance are not known . Overexpression of AtCSP1 (CSDP1; At4g36020) is reported to delay seed germination under dehydration or salt stress conditions, whereas AtCSP2 overexpression accelerates seed germination under salt stress . Juntawong et al. reported that AtCSP1 associates with polyribo-somes via an RNA-mediated interaction. AtCSP1 is implicated in selectively chaperoning mRNAs and improved translation of ribosomal protein mRNAs during cold stress .
Plant cold shock proteins also regulate developmental processes. AtCSP2 is expressed many folds in meristematic tissues and ovules [90,91,92], and regulates flowering transition, and flower and seed development . AtCSP4 (AtGRP2b; At2g21060) also plays an important role in development as AtCSP4 overexpression leads to reduced silique length and induces embryo lethality .
Chaikam and Karlson characterized the cold shock proteins in rice under different stress treatments and during various stages of development . The authors reported that two CSD proteins (OsCSP1 (Os02g0121100) and OsCSP2 (Os08g0129200)) in rice have nucleic acid binding activity and can complement a cold sensitive E. coli strain . Expression of OsCSPs was found at a constant level during cold treatment that last over a period of several days. On the contrary, both OsCSP proteins and transcripts highly accumulated in reproductive tissues and tissues which exhibit meristematic activity . Thus, the role of OsCSPs may be more linked with developmental processes rather than with cold tolerance.
OsCSPs are maintained at a constant level subsequent to a cold treatment lasting over a period of several days.
A time-coursed study through various stages of rice development confirmed that both OsCSP proteins and transcripts are highly accumulated in reproductive tissues and tissues which exhibit meristematic activity. CSP1 associates with polyribosomes (polysomes) via an RNA-mediated interaction.
Plasmodium cold shock proteins
Detection of cold shock protein gene in Plasmodium falciparum genome
Although there is enough information on cold shock proteins of bacteria, humans and plants but the presence of cold shock proteins and their role in the life cycle of Plasmodium falciparum remains largely unknown. Therefore, the existence of cold shock proteins in malaria parasites was identified and their functional relevance was explored through bioinformatics analysis. Uniprot  was used to search P. falciparum genome for presence of cold shock binding genes and a single gene was obtained (Q8I248_PLAF7), indicating the presence of cold shock protein in Plasmodium species. Plasmodb database  was then searched using its Plasmodb ID (PF3D7_0109600), and a putative protein was identified. Sequence analysis and domain organization using Blastp  suggested that P. falciparum cold shock protein (PfCoSP) is 150 amino acids long and harbours a typical N-terminal CSD containing DNA binding site and RNA binding motif (Fig. 1a, b). The PhenoPlasm database  suggested that PfCoSP is essential for survival of the parasite, which underlines its importance in parasite biology and makes this protein an attractive candidate for anti-malarial drug development. Transcriptome analyses from Plasmodb suggest that PfCoSP is upregulated at the mRNA level during gametocyte stages, suggesting the role of this protein during gametocytogenesis (Fig. 1c) . However, presence of PfCoSP transcripts at asexual blood stages and ookinetes also hints its functional role during these stages and therefore should not be ruled out.
The presence of PfCoSP homologues in other species was next investigated. Organism-specific Blastp search using PfCoSP sequence provided its most reliable homologues in Escherichia coli, Homo sapiens and higher plants (Rhodamnia argentea, Vitis vinifera). Multiple sequence alignment of all sequences using Clustal omega  indicates similarity among cold shock protein domain only. Multiple sequence alignment was generated using the cold shock protein domain regions of all the sequences and a phylogenetic tree was constructed to investigate the sequence relationships among these cold shock proteins . Predicted residues comprising the DNA binding site and RNA binding motif in PfCoSP were found to be moderately conserved among its homologues in bacteria, humans and plants (Fig. 1d). Phylogenetic tree suggests that PfCoSP and its homologues are grouped into 3 branches where PfCoSP was more closely related to human cold shock protein ‘CRHSP-24′ and distantly related to Escherichia coli cold shock proteins (CspA, CspG, CspE) (Fig. 1e).
PfCoSP homologues in other Plasmodium species
The presence of PfCoSP homologues in other Plasmodium species were detected using organism-specific Blastp search . The amino acid sequence of PfCoSP was used to scan the genome sequences from two other primate parasites (Plasmodium vivax and Plasmodium knowlesi) and from 3 rodent parasites (Plasmodium chabaudi, Plasmodium berghei and Plasmodium yoelii). PfCoSP homologues in all these Plasmodium species were identified. This indicates the existence of cold shock proteins in other Plasmodium species apart from malaria parasites. Table 1 shows the amino acid sequence identity between PfCoSP and its corresponding sequence in other Plasmodium species.
Multiple sequence alignment showed that the predicted residues comprising the DNA and RNA binding motifs in PfCoSP are highly conserved among its homologues in Plasmodium species (Fig. 2a). A phylogenetic tree shows grouping of primate parasite homologues and rodent parasite homologues (Fig. 2b). PfCoSP was also found to be conserved among other protozoans, such as Cryptosporidium parvum and Toxoplasma gondii, as well as in unrelated organisms, such as Drosophila melanogaster, Caenorhabditis elegans, Anopheles gambiae, Arabidopsis thaliana, and Oryza sativa (Fig. 2c).
In silico structural characterization of Plasmodium cold shock proteins
To gain insight into the functional role of Plasmodium cold shock proteins, their three dimensional structures were first predicted and compared with solved structure of human YB-1. The homology modelling approach was followed to predict the structure of PfCoSP and its homologues in P. vivax and P. berghei. Blast search in Protein Data Bank identified the template for cold shock protein domain only for these cold shock proteins . Structure of Salmonella typhi cold shock protein (PDB Id: 3I2Z) was used as template for modelling cold shock protein domain (28–73 amino acid residues) of PfCoSP while cold shock protein A from Corynebacterium pseudotuberculosis (PDB Id: 506F) was used for modelling cold shock protein domain of P. vivax (PVBG_03557; 34–102 amino acid residues) and P. berghei (PBANKA_020400; 36–85 amino acid residues). All the modelled structures were obtained using Modeller 9.14  and refined using 3D refine . 3D refine follows stepwise refinement protocol based on optimizing hydrogen bonding network and atomic-level energy minimization for improving the global and local structural quality measures . Tests such as Ramachandran plot  and Errat  were run on the generated models to assess their acceptability, and were found suitable for structural analysis (Table 2). Ramachandran plot provides the stereo-chemical evaluation of backbone psi and phi dihedral angles  whereas Errat examines the statistics of non-bonded interactions between different atom types, and reveals the overall model quality. Generally accepted range for the good quality model is > 50. Plasmodium cold shock proteins were observed to comprise of OB-fold that consist of antiparallel beta strands forming beta barrel (Fig. 3a). This indicates that Plasmodium cold shock proteins are structurally conserved and have similar architecture as those of E. coli and human cold shock proteins.
A recent study by Yang et al. solved the crystal structure of a human Y-box binding protein 1 (YB-1)-RNA complex and reveals key residues that participate in RNA binding . YB-1 is a member of the CSD protein family and is recognized as an oncogenic factor in several solid tumours. It binds with RNA and plays role in several steps of post-transcriptional regulation of gene expression, including mRNA splicing, stability, and translation, microRNA processing, and stress granule assembly .
Multiple sequence alignment of human YB-1 with PfCoSP and its homologues in Plasmodium species was performed and found that most of the residues of human YB-1 that participate in RNA binding (K64, W65, N67, N70, Y72, F74, D83, F85, H87, T89, D105, K118, A120) are conserved in Plasmodium cold shock proteins (Fig. 3b). Yang et al. also revealed that YB-1 CSD forms a homodimer in solution, and the residues responsible for dimerization include F66, N67, V68, Y99, D105, and E107. Out of these, Tyr-99 and Asp-105 are critical for YB-1 CSD dimerization. When Tyr-99 and Asp-105 are substituted with Ala, this mutant exhibited a dramatic decrease in the interactions responsible for dimer formation. Also, it resulted in reduced RNA binding activity of YB-1, and abrogated the splicing activation of YB-1 targets. Using these data, the oligomerization state of Plasmodium cold shock proteins was explored. Multiple sequence alignment showed that F66 of human YB-1 was fully conserved in Plasmodium cold shock proteins while N67, D105, E107 were semi-conserved. However, V68 and Y99 of human YB-1 were not conserved in Plasmodium cold shock proteins. Since Y99 is one of the key residues for YB-1 dimerization and is not conserved in Plasmodium cold shock proteins, it is presumed that PfCoSP and its homologues in Plasmodium species may exist as monomeric structures. Such striking structural differences between host and parasite protein counterparts may identify essential ‘PfCoSP’ as a candidate for structure-based drug design against falciparum malaria. PfCoSP monomeric state, however, needs to be confirmed in vivo and in vitro to conclude this. Mapping of the residues on surface representation of human YB-1, PfCoSP and its homologues in P. berghei and P. vivax are shown in Fig. 3c.
Docking of PfCoSP with BDNA and RNA oligo ‘UCAUGU’
Nucleic-acid binding ability of PfCoSP was next investigated by docking its modelled structure with BDNA and RNA oligo ‘UCAUGU’ using PatchDock  and HDOCK servers , respectively. Docking was performed by considering the corresponding residues as active sites in PfCoSP that were reported RNA binding residues in YB-1 by Yang et al. , while no residue was given as active site in docking PfCoSP with BDNA. Docking energy for PfCoSP-BDNA and PfCoSP-RNA complex were observed to be −216 and −236.54 kJ/mol respectively, indicating the stability of the docked structures. PfCoSP-BDNA and PfCoSP-RNA docked complex along with that of YB-1 are shown in Fig. 4a. To identify key residues involved in interactions, the residue interaction network (RIN) profiles of docked complexes were generated using RING 2.0 web server . RIN provides a visual interface to evaluate the stability of connections formed by amino acid residues at the contact sites . Detail analysis of RIN plot suggested that His58 and Tyr59 of PfCoSP form maximum number of interactions with both BDNA and RNA. Also, Phe45 and Phe56 were greatly involved in forming the network of PfCoSP with RNA. These results are coherent with a previous report where corresponding residues of His58, Phe45 and Phe56 in YB-1 were reported to be critical for RNA binding by the CSD of YB-1 . Various interactions in the form of a detailed network model are represented in Fig. 4b.
Functional aspects of PfCoSP
An attempt was made to explore the functional aspects of PfCoSP in the malaria parasite. In silico analysis was performed using the MEME suite tool  to identify motifs that can be correlated with the functional role of PfCoSP in malaria parasites. The search identified 3 motifs ‘WNANMDITQ’, ‘LRRKIH’ and ‘HFNSYK’ in PfCoSP. These motifs were searched in protein sequence databases by using Find Individual Motif Occurrences (FIMO) . Site-specific DNA methytransferases, phosphatidylinositol 4-kinases and homeobox protein were found as significant matches for motifs WNANMDITQ, LRRKIH and HFNSYK, respectively (Table 3). Interestingly, all these proteins/enzymes are DNA or nucleotide-binding proteins. DNA methytransferases and homeobox proteins play a key role in regulating gene expression while phosphatidylinositol 4-kinases modulate inter-organelle lipid trafficking and phosphoinositide signalling [112,113,114]. These in silico data hint that PfCoSP may have a role in controlling gene expression and regulating lipid trafficking by its nuclei acid binding ability.
Parasite life cycle and PfCoSP
Complex and multi-stage life cycle of the malaria parasite involves two hosts, humans and female Anopheles mosquitoes. The majority of circulating parasites in an infected human are asexually dividing merozoites . A small portion of these undergo a differentiation pathway and a series of changes, which lead to the generation of a sexually competent parasite called ‘gametocyte’ . This maturation is called gametocytogenesis which involves formation of pre-gametes that later fertilize in the mosquito to complete the sexual cycle. Transmission from an infected human host to a susceptible mosquito occurs through these highly specialized gametocytes. After a mosquito feeds on an infected host, gametocytes egress from their host erythrocytes to initiate gametogenesis within the mosquito midgut lumen. Female gametocytes produce a single non-motile spherical female gamete, while male gametocytes undergo ‘exflagellation’, a process that results in the production of 8 motile male gametes .
As P. falciparum gametocytes switch from human host to female Anopheles, it results in transitioning from the relatively protected environment within the human erythrocytes to being an exposed parasite in the lumen of a mosquito. Apart from the fact that the parasite becomes extracellular, there is a modified pH and, importantly, drop in temperature . It is obvious that the parasite prepares itself for upcoming environmental change. Transcriptome analyses suggest that ~ 300 genes are upregulated at the mRNA level during gametocyte development [117, 118]. In silico analysis identified a cold shock protein in malaria parasite (PfCoSP) whose transcriptome data also suggest that it is upregulated at gametocyte stages . PfCoSP is reported to be essential for parasite survival . This hints that PfCoSP may play its essential role in egress machinery of gametocytes by regulating gene expression of pivotal genes that are involved during gametocytogenesis. Apart from the gametocyte stages where the role of PfCoSP can be related to temperature difference phenotype, PfCoSP transcripts are also found at ookinete and asexual blood stages of malaria parasite. This further suggests that PfCoSP may play its functional role at other stages of parasite life cycle.
This review highlights the significance of cold shock proteins in several organisms and sheds new light on the unexplored cold shock protein member of P. falciparum. Functional diversity of cold shock protein family is entailed by discussing their known roles in gene expression regulation, cold adaptation, disease progression, and developmental processes such as flowering transition and flower and seed development. In silico work described here provide structural information of PfCoSP and hints its functional role particularly in regulating gene expression at gametocyte stages. However, the presence and structure–function characterization of PfCoSP needs to be confirmed in vivo and in vitro to conclude its role in gametocytogenesis and also at other stages of parasite life cycle. Future studies should aim at the structural and functional characterization of PfCoSP to understand its pivotal role in malaria parasites. Since cold shock proteins are verifiable targets for therapeutic intervention, the work described here, along with future studies on PfCoSP, may help with strategies aimed at targeting this protein directly for the development of anti-malarials and transmission-blocking vaccines.
Availability of data and materials
Cold shock domain
Y-box binding protein 1
- PfCoSP :
Plasmodium falciparum Cold shock protein
Calcium-regulated heat-stable protein 1
Yamanaka K, Fang L, Inouye M. The CspA family in Escherichia coli: multiple gene duplication for stress adaptation. Mol Microbiol. 1998;27:247–55.
Ermolenko DN, Makhatadze GI. Bacterial cold-shock proteins. Cell Mol Life Sci. 2002;59:1902–13.
Weber MH, Marahiel MA. Bacterial cold shock responses. Sci Prog. 2003;86:9–75.
Phadtare S. Recent developments in bacterial cold-shock response. Curr Issues Mol Biol. 2004;6:125–36.
Wolffe AP, Tafuri S, Ranjan M, Familari M. The Y-box factors: a family of nucleic acid binding proteins conserved from Escherichia coli to man. New Biol. 1992;4:290–8.
Lindquist JA, Brandt S, Bernhardt A, Zhu C, Mertens PR. The role of cold shock domain proteins in inflammatory diseases. J Mol Med. 2014;92:207–16.
Brandt S, Raffetseder U, Djudjaj S, Schreiter A, Kadereit B, Michele M, et al. Cold shock Y-box protein-1 participates in signaling circuits with auto-regulatory activities. Eur J Cell Biol. 2012;91:464–71.
Wolffe AP. Structural and functional properties of the evolutionarily ancient Y-box family of nucleic acid binding proteins. BioEssays. 1994;16:245–51.
Jiang W, Hou Y, Inouye M. CspA, the major cold-shock protein of Escherichia coli, is an RNA chaperone. J Biol Chem. 1997;272:196–202.
Bae W, Xia B, Inouye M, Severinov K. Escherichia coli CspA-family RNA chaperones are transcription antiterminators. Proc Natl Acad Sci USA. 2000;97:7784–9.
Phadtare S, Inouye M, Severinov K. The nucleic acid melting activity of Escherichia coli CspE is critical for transcription antitermination and cold acclimation of cells. J Biol Chem. 2002;277:7239–45.
Jones PG, Inouye M. The cold-shock response—a hot topic. Mol Microbiol. 1994;11:811–8.
Gottesman S. Chilled in translation: adapting to bacterial climate change. Mol Cell. 2018;70:193–4.
Jin B, Jeong KW, Kim Y. Structure and flexibility of the thermophilic cold-shock protein of Thermus aquaticus. Biochem Biophys Res Commun. 2014;451:402–7.
Perl D, Welker C, Schindler T, Schröder K, Marahiel MA, Jaenicke R, Schmid FX. Conservation of rapid two-state folding in mesophilic, thermophilic and hyperthermophilic cold shock proteins. Nat Struct Biol. 1998;5:229–35.
Lopez MM, Yutani K, Makhatadze GI. Interactions of the major cold shock protein of Bacillus subtilis CspB with single-stranded DNA templates of different base composition. J Biol Chem. 1999;274:33601–8.
Lopez MM, Makhatadze GI. Major cold shock proteins, CspA from Escherichia coli and CspB from Bacillus subtilis, interact differently with single-stranded DNA templates. Biochim Biophys Acta Prot Struct Mol Enzym. 2000;1479:196–202.
Lopez MM, Yutani K, Makhatadze GI. Interactions of the Cold Shock Protein CspB from Bacillus subtilis with Single-stranded DNA. Importance of the T base content and position within the template. J Biol Chem. 2001;276:15511–8.
Zeeb M, Balbach J. Single-stranded DNA binding of the cold-shock protein CspB from Bacillus subtilis: NMR mapping and mutational characterization. Protein Sci. 2003;12:112–23.
Landsman D. RNP-1, an RNA-binding motif is conserved in the DNA-binding cold shock domain. Nucleic Acids Res. 1992;20:2861–4.
Burd CG, Dreyfuss G. Conserved structures and diversity of functions of RNA-binding proteins. Science. 1994;265:615–21.
Schröder K, Graumann P, Schnuchel A, Holak TA, Marahiel MA. Mutational analysis of the putative nucleic acid-binding surface of the cold-shock domain, CspB, revealed an essential role of aromatic and basic residues in binding of single-stranded DNA containing the Y-box motif. Mol Microbiol. 1995;16:699–708.
Charollais J, Dreyfus M, Iost I. CsdA, a cold-shock RNA helicase from Escherichia coli, is involved in the biogenesis of 50S ribosomal subunit. Nucleic Acids Res. 2004;32:2751–9.
Phadtare S. Escherichia coli cold-shock gene profiles in response to over-expression/deletion of CsdA, RNase R and PNase and relevance to low-temperature RNA metabolism. Genes Cells. 2012;17:850–74.
Jones PG, VanBogelen RA, Neidhardt FC. Induction of proteins in response to low temperature in Escherichia coli. J Bacteriol. 1987;169:2092–5.
Yamanaka K, Mitani T, Ogura T, Niki H, Hiraga S. Cloning, sequencing, and characterization of multicopy suppressors of a mukB mutation in Escherichia coli. Mol Microbiol. 1994;13:301–12.
Etchegaray JP, Jones PG, Inouye M. Differential thermoregulation of two highly homologous cold-shock genes, cspA and cspB, of Escherichia coli. Genes Cells. 1996;1:171–8.
Nakashima K, Kanamaru K, Mizuno T, Horikoshi K. A novel member of the cspA family of genes that is induced by cold shock in Escherichia coli. J Bacteriol. 1996;178:2994–7.
Wang N, Yamanaka K, Inouye M. CspI, the ninth member of the CspA family of Escherichia coli, is induced upon cold shock. J Bacteriol. 1999;181:1603–9.
Uppal S, Rao Akkipeddi VS, Jawali N. Posttranscriptional regulation of cspE in Escherichia coli: involvement of the short 5′-untranslated region. FEMS Microbiol Lett. 2008;279:83–91.
Xia B, Ke H, Inouye M. Acquirement of cold sensitivity by quadruple deletion of the cspA family and its suppression by PNPase S1 domain in Escherichia coli. Mol Microbiol. 2001;40:179–88.
Yamanaka K, Inouye M. Growth-phase-dependent expression of cspD, encoding a member of the CspA family in Escherichia coli. J Bacteriol. 1997;179:5126–30.
Yamanaka K, Zheng W, Crooke E, Wang YH, Inouye M. CspD, a novel DNA replication inhibitor induced during the stationary phase in Escherichia coli. Mol Microbiol. 2001;39:1572–84.
Czapski TR, Trun N. Expression of csp genes in E. coli K-12 in defined rich and defined minimal media during normal growth, and after cold-shock. Gene. 2014;547:91–7.
Phadtare S, Inouye M. Role of CspC and CspE in regulation of expression of RpoS and UspA, the stress response proteins in Escherichia coli. J Bacteriol. 2001;183:1205–14.
Kim Y, Wang X, Zhang XS, Grigoriu S, Page R, Peti W, Wood TK. Escherichia coli toxin/antitoxin pair MqsR/MqsA regulate toxin CspD. Environ Microbiol. 2010;12:1105–21.
Li HT, Liu H, Gao XS, Zhang H. Knock-out of Arabidopsis AtNHX4 gene enhances tolerance to salt stress. Biochem and Biophys Res Commun. 2009;382:637–41.
Goldstein J, Pollitt NS, Inouye M. Major cold shock protein of Escherichia coli. Proc Natl Acad Sci. 1990;87:283–7.
Giuliodori AM, Di Pietro F, Marzi S, Masquida B, Wagner R, Romby P, et al. The cspA mRNA is a thermosensor that modulates translation of the cold-shock protein CspA. Mol Cell. 2010;37:21–33.
Mega R, Manzoku M, Shinkai A, Nakagawa N, Kuramitsu S, Masui R. Very rapid induction of a cold shock protein by temperature downshift in Thermus thermophilus. Biochem Biophys Res Commun. 2010;399:336–40.
Mitta M, Fang L, Inouye M. Deletion analysis of cspA of Escherichia coli: requirement of the AT-rich UP element for cspA transcription and the downstream box in the coding region for its cold shock induction. Mol Microbiol. 1997;26:321–35.
Phadtare S, Severinov K. Extended−10 motif is critical for activity of the cspA promoter but does not contribute to low-temperature transcription. J Bacteriol. 2005;187:6584–9.
Graumann P, Wendrich TM, Weber MH, Schröder K, Marahiel MA. A family of cold shock proteins in Bacillus subtilis is essential for cellular growth and for efficient protein synthesis at optimal and low temperatures. Mol Microbiol. 1997;25:741–56.
Kremer W, Schuler B, Harrieder S, Geyer M, Gronwald W, Welker C, et al. Solution NMR structure of the cold-shock protein from the hyperthermophilic bacterium Thermotoga maritima. Eur J Biochem. 2001;268:2527–39.
Jung A, Bamann C, Kremer W, Kalbitzer HR, Brunner E. High-temperature solution NMR structure of TmCsp. Protein Sci. 2004;13:342–50.
Schindelin H, Marahiel MA, Heinemann U. Universal nucleic acid-binding domain revealed by crystal structure of the B subtilis major cold-shock protein. Nature. 1993;364:164–8.
Schindelin H, Jiang W, Inouye M, Heinemann U. Crystal structure of CspA, the major cold shock protein of Escherichia coli. Proc Natl Acad Sci USA. 1994;91:5119–23.
Theobald DL, Mitton-Fry RM, Wuttke DS. Nucleic acid recognition by OB-fold proteins. Annu Rev Biophys Biomol Struct. 2003;32:115–33.
Lei M, Podell ER, Cech TR. Structure of human POT1 bound to telomeric single-stranded DNA provides a model for chromosome end-protection. Nat Struct Mol Biol. 2004;11:1223–9.
Mitton-Fry RM, Anderson EM, Theobald DL, Glustrom LW, Wuttke DS. Structural basis for telomeric single-stranded DNA recognition by yeast Cdc13. J Mol Biol. 2004;338:241–55.
Lee J, Jeong KW, Jin B, Ryu KS, Kim EH, Ahn JH, Kim Y. Structural and dynamic features of cold-shock proteins of Listeria monocytogenes, a psychrophilic bacterium. Biochemistry. 2013;52:2492–504.
Lindquist JA, Mertens PR. Cold shock proteins: from cellular mechanisms to pathophysiology and disease. Cell Commun Signal. 2018;16:63.
Didier DK, Schiffenbauer J, Woulfe SL, Zacheis M, Schwartz BD. Characterization of the cDNA encoding a protein binding to the major histocompatibility complex class II Y box. Proc Natl Acad Sci USA. 1988;85:7322–6.
Horwitz EM, Maloney KA, Ley TJ. A human protein containing a" cold shock" domain binds specifically to H-DNA upstream from the human gamma-globin genes. J Biol Chem. 1994;269:14130–9.
Chen CY, Gherzi R, Andersen JS, Gaietta G, Jürchott K, Royer HD, et al. Nucleolin and YB-1 are required for JNK-mediated interleukin-2 mRNA stabilization during T-cell activation. Gene Dev. 2000;14:1236–48.
Capowski EE, Esnault S, Bhattacharya S, Malter JS. Y box-binding factor promotes eosinophil survival by stabilizing granulocyte-macrophage colony-stimulating factor mRNA. J Immunol. 2001;167:5970–6.
Gaudreault I, Guay D, Lebel M. YB-1 promotes strand separation in vitro of duplex DNA containing either mispaired bases or cisplatin modifications, exhibits endonucleolytic activities and binds several DNA repair proteins. Nucleic Acids Res. 2004;32:316–27.
Chattopadhyay R, Das S, Maiti AK, Boldogh I, Xie J, Hazra TK, et al. Regulatory role of human AP-endonuclease (APE1/Ref-1) in YB-1-mediated activation of the multidrug resistance gene MDR1. Mol Cell Biol. 2008;28:7066–80.
Chen X, Li A, Sun BF, Yang Y, Han YN, Yuan X, et al. 5-methylcytosine promotes pathogenesis of bladder cancer through stabilizing mRNAs. Nat Cell Biol. 2019;21:978–90.
Ohga T, Uchiumi T, Makino Y, Koike K, Wada M, Kuwano M, et al. Direct involvement of the Y-box binding protein YB-1 in genotoxic stress-induced activation of the human multidrug resistance 1 gene. J Biol Chem. 1998;273:5997–6000.
Eliseeva IA, Kim ER, Guryanov SG, Ovchinnikov LP, Lyabin DN. Y-box-binding protein 1 (YB-1) and its functions. Biochem. 2011;76:1402–33.
Koike K, Uchiumi T, Ohga T, Toh S, Wada M, Kohno K, et al. Nuclear translocation of the Y-box binding protein by ultraviolet irradiation. FEBS Lett. 1997;417:390–4.
Bargou RC, Jürchott K, Wagener C, Bergmann S, Metzner S, Bommert K, et al. Nuclear localization and increased levels of transcription factor YB-1 in primary human breast cancers are associated with intrinsic MDR1 gene expression. Nat Med. 1997;3:447–50.
Oda Y, Ohishi Y, Saito T, Hinoshita E, Uchiumi T, Kinukawa N, et al. Nuclear expression of Y-box-binding protein-1 correlates with P-glycoprotein and topoisomerase II alpha expression, and with poor prognosis in synovial sarcoma. J Pathol. 2003;199:251–8.
Pfeiffer JR, McAvoy BL, Fecteau RE, Deleault KM, Brooks SA. CARHSP1 is required for effective tumor necrosis factor alpha mRNA stabilization and localizes to processing bodies and exosomes. Mol Cell Biol. 2011;31:277–86.
Groblewski GE, Yoshida M, Bragado MJ, Ernst SA, Leykam J, Williams JA. Purification and characterization of a novel physiological substrate for calcineurin in mammalian cells. J Biol Chem. 1998;273:22738–44.
Castiglia D, Scaturro M, Nastasi T, Cestelli A, Di Liegro I. PIPPin, a putative RNA-binding protein specifically expressed in the rat brain. Biochem Biophys Res Commun. 1996;218:390–4.
Nastasi T, Scaturro M, Bellafiore M, Raimondi L, Beccari S, Cestelli A, et al. PIPPin is a brain-specific protein that contains a cold-shock domain and binds specifically to H1 and H33 mRNAs. J Biol Chem. 1999;274:24087–93.
Di Liegro CM, Schiera G, Proia P, Saladino P, Di Liegro I. Identification in the rat brain of a set of nuclear proteins interacting with H1 mRNA. Neuroscience. 2013;229:71–6.
Anderson EC, Catnaigh PÓ. Regulation of the expression and activity of Unr in mammalian cells. Biochem Soc Trans. 2015;43:1241–6.
Jeffers M, Paciucci R, Pellicer A. Characterization of unr; a gene closely linked to N-ras. Nucleic Acids Res. 1990;18:4891.
Jeffers M, Pellicer A. Multiple intragenic elements regulate the expression of the murine N-ras gene. Oncogene. 1992;7:2115–23.
Jacquemin-Sablon H, Dautry F. Organization of the unrl N-ras locus: characterization of the promoter region of the human unr gene. Nucleic Acids Res. 1992;20:6355–61.
Jacquemin-Sablon H, Triqueneaux G, Deschamps S, le Maire M, Doniger J, Dautry F. Nucleic acid binding and intracellular localization of unr, a protein with five cold shock domains. Nucleic Acids Res. 1994;22:2643–50.
Doniger J, Landsman D, Gonda MA, Wistow G. The product of unr, the highly conserved gene upstream of N-ras, contains multiple repeats similar to the cold-shock domain (CSD), a putative DNA-binding motif. New Biol. 1992;4:389–95.
Guo AX, Cui JJ, Wang LY, Yin JY. The role of CSDE1 in translational reprogramming and human diseases. Cell Commun Signal. 2020;18:14.
Balzeau J, Menezes MR, Cao S, Hagan JP. The LIN28/let-7 pathway in cancer. Front Genet. 2017;8:31.
Jin J, Jing W, Lei XX, Feng C, Peng S, Boris-Lawrie K, Huang Y. Evidence that Lin28 stimulates translation by recruiting RNA helicase A to polysomes. Nucleic Acids Res. 2011;39:3724–34.
Heo I, Joo C, Cho J, Ha M, Han J, Kim VN. Lin28 mediates the terminal uridylation of let-7 precursor MicroRNA. Mol Cell. 2008;32:276–84.
Heo I, Joo C, Kim YK, Ha M, Yoon MJ, Cho J, et al. TUT4 in concert with Lin28 suppresses microRNA biogenesis through pre-microRNA uridylation. Cell. 2009;138:696–708.
Piskounova E, Polytarchou C, Thornton JE, LaPierre RJ, Pothoulakis C, Hagan JP, et al. Lin28A and Lin28B inhibit let-7 microRNA biogenesis by distinct mechanisms. Cell. 2011;147:1066–79.
Sasaki K, Imai R. Pleiotropic roles of cold shock domain proteins in plants. Front Plant Sci. 2012;2:116.
Karlson D, Nakaminami K, Toyomasu T, Imai R. A cold-regulated nucleic acid-binding protein of winter wheat shares a domain with bacterial cold shock proteins. J Biol Chem. 2002;277:35248–56.
Nakaminami K, Sasaki K, Kajita S, Takeda H, Karlson D, Ohgi K, Imai R. Heat stable ssDNA/RNA-binding activity of a wheat cold shock domain protein. FEBS Lett. 2005;579:4887–91.
Nakaminami K, Karlson DT, Imai R. Functional conservation of cold shock domains in bacteria and higher plants. Proc Natl Acad Sci USA. 2006;103:10122–7.
Radkova M, Vítámvás P, Sasaki K, Imai R. Development-and cold-regulated accumulation of cold shock domain proteins in wheat. Plant Physiol Biochem. 2014;77:44–8.
Kim MH, Sasaki K, Imai R. Cold shock domain protein 3 regulates freezing tolerance in Arabidopsis thaliana. J Biol Chem. 2009;284:23454–60.
Park SJ, Kwak KJ, Oh TR, Kim YO, Kang H. Cold shock domain proteins affect seed germination and growth of Arabidopsis thaliana under abiotic stress conditions. Plant Cell Physiol. 2009;50:869–78.
Juntawong P, Sorenson R, Bailey-Serres J. Cold shock protein 1 chaperones mRNA s during translation in Arabidopsis thaliana. Plant J. 2013;74:1016–28.
Fusaro AF, Bocca SN, Ramos RL, Barrôco RM, Magioli C, Jorge VC, et al. AtGRP2, a cold-induced nucleo-cytoplasmic RNA-binding protein, has a role in flower and seed development. Planta. 2007;225:1339–51.
Sasaki K, Kim MH, Imai R. Arabidopsis cold shock domain protein2 is a RNA chaperone that is regulated by cold and developmental signals. Biochem Biophys Res Commun. 2007;364:633–8.
Nakaminami K, Hill K, Perry SE, Sentoku N, Long JA, Karlson DT. Arabidopsis cold shock domain proteins: relationships to floral and silique development. J Exp Bot. 2009;60:1047–62.
Yang Y, Karlson DT. Overexpression of AtCSP4 affects late stages of embryo development in Arabidopsis. J Exp Bot. 2011;62:2079–91.
Chaikam V, Karlson D. Functional characterization of two cold shock domain proteins from Oryza sativa. Plant Cell Environ. 2008;31:995–1006.
UniProt Consortium. UniProt: a worldwide hub of protein knowledge. Nucleic Acids Res. 2019;47:D506–15.
Aurrecoechea C, Brestelli J, Brunk BP, Dommer J, Fischer S, Gajria B, et al. PlasmoDB: a functional genomic database for malaria parasites. Nucleic Acids Res. 2009;37:D539–43.
Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997;25:3389–402.
Sanderson T, Rayner JC. PhenoPlasm: a database of disruption phenotypes for malaria parasite genes. Wellcome Open Res. 2017;2:45.
López-Barragán MJ, Lemieux J, Quiñones M, Williamson KC, Molina-Cruz A, Cui K, et al. Directional gene expression and antisense transcripts in sexual and asexual stages of Plasmodium falciparum. BMC Genom. 2011;12:587.
Sievers F, Wilm A, Dineen D, Gibson TJ, Karplus K, Li W, et al. Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. Mol Syst Biol. 2011;7:539.
Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, et al. The Protein Data Bank. Nucleic Acids Res. 2000;28:235–42.
Šali A, Blundell TL. Comparative protein modelling by satisfaction of spatial restraints. J Mol Biol. 1993;234:779–815.
Bhattacharya D, Cheng J. 3Drefine: Consistent protein structure refinement by optimizing hydrogen bonding network and atomic-level energy minimization. Proteins. 2013;81:119–31.
Lovell SC, Davis IW, Arendall WB III, De Bakker PI, Word JM, Prisant MG, et al. Structure validation by Cα geometry: ϕ, ψ and Cβ deviation. Proteins. 2003;50:437–50.
Colovos C, Yeates TO. Verification of protein structures: patterns of nonbonded atomic interactions. Protein Sci. 1993;2:1511–9.
Yang XJ, Zhu H, Mu SR, Wei WJ, Yuan X, Wang M, Liu Y, et al. Crystal structure of a Y-box binding protein 1 (YB-1)–RNA complex reveals key features and residues interacting with RNA. J Biol Chem. 2019;294:10998–1010.
Inbar Y, Nussinov R, Wolfson HJ. PatchDock and SymmDock: servers for rigid and symmetric docking. Nucleic Acids Res. 2005;33:W363–7.
Yan Y, Zhang D, Zhou P, Li B, Huang SY. HDOCK: a web server for protein–protein and protein–DNA/RNA docking based on a hybrid strategy. Nucleic Acids Res. 2017;45:W365–73.
Piovesan D, Minervini G, Tosatto SC. The RING 20 web server for high quality residue interaction networks. Nucleic Acids Res. 2016;44:W367–74.
Bailey TL, Elkan C. Fitting a mixture model by expectation maximization to discover motifs in bipolymers. Proc Int Conf Intell Syst Mol Biol. 1994;2:28–36.
Grant CE, Bailey TL, Noble WS. FIMO: scanning for occurrences of a given motif. Bioinformatics. 2011;27:1017–8.
Jurkowska RZ, Jurkowski TP, Jeltsch A. Structure and function of mammalian DNA methyltransferases. Chem Bio Chem. 2011;12:206–22.
Levine M, Hoey T. Homeobox proteins as sequence-specific transcription factors. Cell. 1988;55:537–40.
Clayton EL, Minogue S, Waugh MG. Mammalian phosphatidylinositol 4-kinases as modulators of membrane trafficking and lipid signaling networks. Prog Lipid Res. 2013;52:294–304.
Cowman AF, Berry D, Baum J. The cellular and molecular basis for malaria parasite invasion of the human red blood cell. J Cell Biol. 2012;198:961–71.
Dearsly AL, Sinden RE, Self IA. Sexual development in malarial parasites: gametocyte production, fertility and infectivity to the mosquito vector. Parasitology. 1990;100:359–68.
Silvestrini F, Bozdech Z, Lanfrancotti A, Di Giulio E, Bultrini E, Picci L, et al. Genome-wide identification of genes upregulated at the onset of gametocytogenesis in Plasmodium falciparum. Mol Biochem Parasitol. 2005;143:100–10.
Young JA, Fivelman QL, Blair PL, de la Vega P, Le Roch KG, Zhou Y, et al. The Plasmodium falciparum sexual development transcriptome: a microarray analysis using ontology-based pattern identification. Mol Biochem Parasitol. 2005;143:67–79.
Funding from Science and Engineering Research Board (SERB) and the National Bioscience Award from DBT for SS is acknowledged. AB is supported by National Post-doctoral fellowship, SERB, India (Fellowship reference no. PDF/2019/000334). VK is supported by Research Associateship Program of Department of Biotechnology, India. MS was funded by a grant from the Russian Foundation for Basic Research No. 19–58-45012.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Behl, A., Kumar, V., Shevtsov, M. et al. Pleiotropic roles of cold shock proteins with special emphasis on unexplored cold shock protein member of Plasmodium falciparum. Malar J 19, 382 (2020). https://doi.org/10.1186/s12936-020-03448-6