AI Article Synopsis

  • The Rep proteins of begomoviruses like CLCuMuV and PeLCV interact with their host's DNA replication machinery, showing 13-28% sequence variation among different virus isolates based on their geographic origins.
  • Yeast two-hybrid assays revealed that the PCNA protein plays a key role in the replication of these viruses by interacting with their Rep proteins.
  • Comparisons of PCNA sequences across species showed high similarity, suggesting a conserved mechanism of Rep protein interaction with eukaryotic PCNA, despite the significant evolutionary differences in their sequences.

Article Abstract

The replication-associated (Rep) proteins of pathogenic begomoviruses, including cotton leaf curl Multan virus (CLCuMuV) and pedilanthus leaf curl virus (PeLCV), interact with the DNA replication machinery of their eukaryotic hosts. The analysis of Rep protein sequences showed that there is 13-28% sequence variation among CLCuMuV and PeLCV isolates, with phylogenetic clusters that can separated at least in part based on the country of origin of the respective viruses. To identify specific host factors involved in the virus replication cycle, we conducted yeast two-hybrid assays to detect possible interactions between the CLCuMuV and PeLCV Rep proteins and 30 protein components of the DNA replication machinery. This showed that the proliferating cell nuclear antigen (PCNA) protein of interacts with Rep proteins from both CLCuMuV and PeLCV. We used the yeast PCNA sequence in BLAST comparisons to identify two PCNA orthologs each in (cotton) (Arabidopsis), and (tobacco). Sequence comparisons showed 38-40% identity between the yeast and plant PCNA proteins, and > 91% identity among the plant PCNA proteins, which clustered together in one phylogenetic group. The expression of the six plant PCNA proteins in the yeast two-hybrid system confirmed interactions with the CLCuMuV and PeLCV Rep proteins. Our results demonstrate that the interaction of begomovirus Rep proteins with eukaryotic PCNA proteins is strongly conserved, despite significant evolutionary variation in the protein sequences of both of the interacting partners.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778653PMC
http://dx.doi.org/10.1007/s13205-020-02499-5DOI Listing

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