Literature DB >> 33430760

Genome-wide identification of the histone acetyltransferase gene family in Triticum aestivum.

Shiqi Gao1,2,3, Linzhi Li2, Xiaolei Han1,2,3, Tingting Liu1, Peng Jin1, Linna Cai1, Miaoze Xu1, Tianye Zhang1, Fan Zhang1, Jianping Chen1, Jian Yang4, Kaili Zhong5.   

Abstract

BACKGROUND: Histone acetylation is a ubiquitous and reversible post-translational modification in eukaryotes and prokaryotes that is co-regulated by histone acetyltransferase (HAT) and histone deacetylase (HDAC). HAT activity is important for the modification of chromatin structure in eukaryotic cells, affecting gene transcription and thereby playing a crucial regulatory role in plant development. Comprehensive analyses of HAT genes have been performed in Arabidopsis thaliana, Oryza sativa, barley, grapes, tomato, litchi and Zea mays, but comparable identification and analyses have not been conducted in wheat (Triticum aestivum).
RESULTS: In this study, 31 TaHATs were identified and divided into six groups with conserved gene structures and motif compositions. Phylogenetic analysis was performed to predict functional similarities between Arabidopsis thaliana, Oryza sativa and Triticum aestivum HAT genes. The TaHATs appeared to be regulated by cis-acting elements such as LTR and TC-rich repeats. The qRT-PCR analysis showed that the TaHATs were differentially expressed in multiple tissues. The TaHATs in expression also responded to temperature changes, and were all significantly upregulated after being infected by barley streak mosaic virus (BSMV), Chinese wheat mosaic virus (CWMV) and wheat yellow mosaic virus (WYMV).
CONCLUSIONS: These results suggest that TaHATs may have specific roles in the response to viral infection and provide a basis for further study of TaHAT functions in T. aestivum plant immunity.

Entities:  

Keywords:  Expression analysis; Genome-wide; Histone acetyltransferases; Temperature; Triticum aestivum; Wheat virus

Mesh:

Substances:

Year:  2021        PMID: 33430760      PMCID: PMC7802222          DOI: 10.1186/s12864-020-07348-6

Source DB:  PubMed          Journal:  BMC Genomics        ISSN: 1471-2164            Impact factor:   3.969


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