Site-Specific Systematic Analysis of Lysine Modification Crosstalk

Proteomics. 2018 May;18(9):e1700292. doi: 10.1002/pmic.201700292. Epub 2018 Apr 16.

Abstract

Research has revealed that post-translational modifications (PTMs) that occur at lysine (PLMs) can cooperatively regulate various biological processes by crosstalk. However, the trend of the crosstalk between multiple PLMs and the properties of PLM crosstalk require additional investigation. Here, the crosstalk among acetylation, succinylation, and SUMOylation is systematically studied in a site-specific waz. First, crosstalk between SUMOylation is detected and succinylation is found to be underexpressed, whereas succinylation tends to crosstalk with acetylation and SUMOylation on the same lysine residue while PLM crosstalk is tissue-specific across different species. Further analysis reveals that different PLMs tend to occur crosstalk at diverse subcellular compartments and structural regions, and they participate in distinct biological processes and functions. Additionally, short-term evolutionary analysis shows that there is no additional evolutionary pressure on PLMs crosstalk sites, as found by comparison with singly modified sites. Finally, phylogenetic classification reveals that genes with co-occupied lysine crosstalk are more likely to have higher evolutionary similarity and possess a tendency to cluster in the specific branch. The integrated approach reported here has the potential for large-scale prioritization of in situ crosstalk of PLM candidates and provides a profound understanding of the underlying relationship between different lysine modifications.

Keywords: SUMOylation; acetylation; amino acid variations; natural selection; protein lysine modifications; succinylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Databases, Protein*
  • Humans
  • Lysine / metabolism*
  • Protein Processing, Post-Translational*
  • Proteins / chemistry*
  • Proteins / metabolism*
  • Succinic Acid / metabolism*
  • Sumoylation*

Substances

  • Proteins
  • Succinic Acid
  • Lysine