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Alternative splicing of a barley gene results in an excess-tillering and semi-dwarf mutant.
Hua, Wei; Tan, Cong; Xie, Jingzhong; Zhu, Jinghuan; Shang, Yi; Yang, Jianming; Zhang, Xiao-Qi; Wu, Xiaojian; Wang, Junmei; Li, Chengdao.
Affiliation
  • Hua W; Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
  • Tan C; Western Barley Genetics Alliance, Murdoch University, Murdoch, WA, 6150, Australia.
  • Xie J; Western Barley Genetics Alliance, Murdoch University, Murdoch, WA, 6150, Australia.
  • Zhu J; State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
  • Shang Y; Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
  • Yang J; Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
  • Zhang XQ; Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
  • Wu X; Western Barley Genetics Alliance, Murdoch University, Murdoch, WA, 6150, Australia.
  • Wang J; Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
  • Li C; Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China. wangjunmei@zaas.ac.cn.
Theor Appl Genet ; 133(1): 163-177, 2020 Jan.
Article in En | MEDLINE | ID: mdl-31690990
ABSTRACT
KEY MESSAGE An excess-tillering semi-dwarf gene Hvhtd was identified from an EMS-induced mutant in barley and alternative splicing results in excess-tillering semi-dwarf traits. Tillering and plant height are important traits determining plant architecture and grain production in cereal crops. This study identified an excess-tillering semi-dwarf mutant (htd) from an EMS-treated barley population. Genetic analysis of the F1, F2, and F23 populations showed that a single recessive gene controlled the excess-tillering semi-dwarf in htd. Using BSR-Seq and gene mapping, the Hvhtd gene was delimited within a 1.8 Mb interval on chromosome 2HL. Alignment of the RNA-Seq data with the functional genes in the interval identified a gene HORVU2Hr1G098820 with alternative splicing between exon2 and exon3 in the mutant, due to a G to A single-nucleotide substitution at the exon and intron junction. An independent mutant with a similar phenotype confirmed the result, with alternative splicing between exon3 and exon4. In both cases, the alternative splicing resulted in a non-functional protein. And the gene HORVU2Hr1G098820 encodes a trypsin family protein and may be involved in the IAA signaling pathway and differs from the mechanism of Green Revolution genes in the gibberellic acid metabolic pathway.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Hordeum / Genes, Plant / Alternative Splicing / Mutation Type of study: Prognostic_studies Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Hordeum / Genes, Plant / Alternative Splicing / Mutation Type of study: Prognostic_studies Language: En Year: 2020 Type: Article