4.3 Article

Interaction of eukaryotic proliferating cell nuclear antigen (PCNA) with the replication-associated protein (Rep) of cotton leaf curl Multan virus and pedilanthus leaf curl virus

Journal

3 BIOTECH
Volume 11, Issue 1, Pages -

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s13205-020-02499-5

Keywords

Cotton; Rep; PCNA; Begomovirus

Funding

  1. International Foundation for Science (IFS) [C/5434-1]
  2. Higher Education Commission (HEC) of Pakistan [1682]
  3. HEC indigenous scholarship program
  4. International Research Support Initiative Program (IRSIP)

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The Rep proteins of pathogenic begomoviruses interact with the DNA replication machinery of their eukaryotic hosts, showing 13-28% sequence variation among CLCuMuV and PeLCV isolates. Although phylogenetic clusters can separate based on the country of origin, interactions with PCNA proteins are strongly conserved across different host species.
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 Saccharomyces cerevisiae DNA replication machinery. This showed that the proliferating cell nuclear antigen (PCNA) protein of S. cerevisiae 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 Gossypium hirsutum (cotton), Arabidopsis thaliana (Arabidopsis), and Nicotiana benthamiana (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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