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mRNA Polyadenylation Machineries in Intestinal Protozoan Parasites
- Ospina‐Villa, Juan David, Tovar‐Ayona, Brisna Joana, López‐Camarillo, César, Soto‐Sánchez, Jacqueline, Ramírez‐Moreno, Esther, Castañón‐Sánchez, Carlos A., Marchat, Laurence A.
- Thejournal of eukaryotic microbiology 2020 v.67 no.3 pp. 306-320
- Cryptosporidium parvum, Entamoeba histolytica, Giardia lamblia, adenosine, diarrhea, gene expression, genes, human health, humans, intestines, messenger RNA, nucleotide sequences, parasites, polymerization, proteins
- In humans, mRNA polyadenylation involves the participation of about 20 factors in four main complexes that recognize specific RNA sequences. Notably, CFIm25, CPSF73, and PAP have essential roles for poly(A) site selection, mRNA cleavage, and adenosine residues polymerization. Besides the relevance of polyadenylation for gene expression, information is scarce in intestinal protozoan parasites that threaten human health. To better understand polyadenylation in Entamoeba histolytica, Giardia lamblia, and Cryptosporidium parvum, which represent leading causes of diarrhea worldwide, genomes were screened for orthologs of human factors. Results showed that Entamoeba histolytica and C. parvum have 16 and 12 proteins out of the 19 human proteins used as queries, respectively, while G. lamblia seems to have the smallest polyadenylation machinery with only six factors. Remarkably, CPSF30, CPSF73, CstF77, PABP2, and PAP, which were found in all parasites, could represent the core polyadenylation machinery. Multiple genes were detected for several proteins in Entamoeba, while gene redundancy is lower in Giardia and Cryptosporidium. Congruently with their relevance in the polyadenylation process, CPSF73 and PAP are present in all parasites, and CFIm25 is only missing in Giardia. They conserve the functional domains and predicted folding of human proteins, suggesting they may have the same roles in polyadenylation.