AI Article Synopsis

  • SET domain-containing proteins are crucial for plant development and stress responses by altering histone methylation.
  • The study identified 52 SET domain-containing genes in Gossypium raimondii, classifying them into seven groups based on conserved sequences and their specific methylation functions.
  • Analysis indicates that gene duplication events and varying expression patterns, particularly under high temperature stress, highlight the evolutionary diversification and potential for resistance genes in economically important cotton species.

Article Abstract

SET (Su(var), E(z), and Trithorax) domain-containing proteins play an important role in plant development and stress responses through modifying lysine methylation status of histone. Gossypium raimondii may be the putative contributor of the D-subgenome of economical crops allotetraploid G. hirsutum and G. barbadense and therefore can potentially provide resistance genes. In this study, we identified 52 SET domain-containing genes from G. raimondii genome. Based on conserved sequences, these genes are grouped into seven classes and are predicted to catalyze the methylation of different substrates: GrKMT1 for H3K9me, GrKMT2 and GrKMT7 for H3K4me, GrKMT3 for H3K36me, GrKMT6 for H3K27me, but GrRBCMT and GrS-ET for nonhistones substrate-specific methylation. Seven pairs of GrKMT and GrRBCMT homologous genes are found to be duplicated, possibly one originating from tandem duplication and five from a large scale or whole genome duplication event. The gene structure, domain organization and expression patterns analyses suggest that these genes' functions are diversified. A few of GrKMTs and GrRBCMTs, especially for GrKMT1A;1a, GrKMT3;3 and GrKMT6B;1 were affected by high temperature (HT) stress, demonstrating dramatically changed expression patterns. The characterization of SET domain-containing genes in G. raimondii provides useful clues for further revealing epigenetic regulation under HT and function diversification during evolution.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013442PMC
http://dx.doi.org/10.1038/srep32729DOI Listing

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