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Published on: October 14, 2022
The m6A writer complex function in main stem apex development by promoting mRNA stability of GIF3, HDA6, and KNAT2/6
Xiaoyu Huang1, Hui Zhang2, Huiping Liao1
1Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Hubei Key Laboratory of Genetic Regulation and Integrative Biology, School of Life Sciences, Central China Normal University, Wuhan, 430079, China.
Abstract:
N6-methyladenosine (m6A) is the most abundant internal posttranscriptional modification of eukaryotic messenger RNA (mRNA), which can be involved in the regulation of mRNA metabolism and processing. Although some progress has been made in understanding the methylation mechanism of mRNA m6A in plants, our knowledge and comprehension of this process in cotton is still significantly limited. In this study, we identified the cotton m6A writers, namely GhMTA-A/D, GhMTB-A/D, and GhFIP37-A/D. These writers are localized within the nucleus. Notably, GhMTA-D has been found to interact with both GhMTB-A and GhFIP37-A. The knockdown of each cotton m6A writer gene, achieved through virus-induced gene silencing, resulted in decreased mRNA m6A levels in cotton main stem apex (MSA). This led to a thicker shoot apical meristem, the formation of an abnormal MSA, and dwarf plants. MeRIP-seq and RNA-seq analyses showed that m6A writers mediate m6A modification and transcripts of mRNAs in cotton MSA by recognizing the motif GGACH and/or GAAGM. Furthermore, m6A writers install m6A in GhGIF3, GhHDA6, and GhKNAT2/6 transcripts, thereby affecting their mRNA stability and regulating MSA development. In summary, our research elucidates a novel mechanism for m6A posttranscriptional regulation and offers valuable insights into the roles of m6A writers in controlling MSA development.
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