Functional Evolution of Phosphatidylethanolamine Binding Proteins in Soybean and Arabidopsis. Issue 2 (6th February 2015)

• Record Type: Journal Article
• Authors: Wang, Zheng; Zhou, Zhengkui; Liu, Yunfeng; Liu, Tengfei; Li, Qing; Ji, Yuanyuan; Li, Congcong; Fang, Chao; Wang, Min; Wu, Mian; Shen, Yanting; Tang, Tian; Ma, Jianxin; Tian, Zhixi
• Is Part Of: The Plant Cell. Volume 27:Issue 2(2015)
• Page Start: 323
• Page End: 336
• Publication Date: 2015-02-06
• DOI: 10.1105/tpc.114.135103
• Languages: English
• ISSNs: 1040-4651

Abstract

Abstract : Functional analysis identifies amino acid substitutions causing PEBP functional evolution and shows the importance of coding sequence divergence in driving functional divergence of duplicated genes. Abstract: Gene duplication provides resources for novel gene functions. Identification of the amino acids responsible for functional conservation and divergence of duplicated genes will strengthen our understanding of their evolutionary course. Here, we conducted a systemic functional investigation of phosphatidylethanolamine binding proteins (PEBPs) in soybean ( Glycine max ) and Arabidopsis thaliana . Our results demonstrated that after the ancestral duplication, the lineage of the common ancestor of the FLOWERING LOCUS T ( FT ) and TERMINAL FLOWER1 ( TFL1 ) subfamilies functionally diverged from the MOTHER OF FT AND TFL1 ( MFT ) subfamily to activate flowering and repress flowering, respectively. They also underwent further specialization after subsequent duplications. Although the functional divergence increased with duplication age, we observed rapid functional divergence for a few pairs of young duplicates in soybean. Association analysis between amino acids and functional variations identified critical amino acid residues that led to functional differences in PEBP members. Using transgenic analysis, we validated a subset of these differences. We report clear experimental evidence for the functional evolution of the PEBPs in the MFT, FT, and TFL1 subfamilies, which predate the origin of angiosperms. Our results highlight the role of amino acid divergence in driving evolutionary novelty after duplication.