A homolog of splicing factor SF1 is essential for development and is involved in the alternative splicing of pre-mRNA in Arabidopsis thaliana

被引:52
作者
Jang, Yun Hee [1 ]
Park, Hyo-Young [1 ]
Lee, Keh Chien [1 ]
Thu, May Phyo [1 ]
Kim, Soon-Kap [1 ]
Suh, Mi Chung [2 ]
Kang, Hunseung [3 ]
Kim, Jeong-Kook [1 ]
机构
[1] Korea Univ, Sch Life Sci & Biotechnol, Plant Signaling Network Res Ctr, Seoul 136701, South Korea
[2] Chonnam Natl Univ, Dept Bioenergy Sci & Technol, Kwangju 500757, South Korea
[3] Chonnam Natl Univ, Div Plant Biotechnol, Kwangju 500757, South Korea
基金
新加坡国家研究基金会;
关键词
alternative splicing; SF1; development; abnormal abscisic acid; Arabidopsis thaliana Heynh; PROTEIN-PROTEIN INTERACTIONS; ACID SIGNAL-TRANSDUCTION; CAP-BINDING PROTEIN; PLANT DEVELOPMENT; SCHIZOSACCHAROMYCES-POMBE; SACCHAROMYCES-CEREVISIAE; SR45; PROTEIN; IN-VIVO; YEAST; COMPLEX;
D O I
10.1111/tpj.12491
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
During initial spliceosome assembly, SF1 binds to intron branch points and interacts with U2 snRNP auxiliary factor 65 (U2AF65). Here, we present evidence indicating that AtSF1, the Arabidopsis SF1 homolog, interacts with AtU2AF65a and AtU2AF65b, the Arabidopsis U2AF65 homologs. A mutant allele of AtSF1 (At5g51300) that contains a T-DNA insertion conferred pleiotropic developmental defects, including early flowering and abnormal sensitivity to abscisic acid. An AtSF1 promoter-driven GUS reporter assay showed that AtSF1 promoter activity was temporally and spatially altered, and that full AtSF1 promoter activity required a significant proportion of the coding region. DNA chip analyses showed that only a small proportion of the transcriptome was altered by more than twofold in either direction in the AtSF1 mutant. Expression of the mRNAs of many heat shock proteins was more than fourfold higher in the mutant strain; these mRNAs were among those whose expression was increased most in the mutant strain. An RT-PCR assay revealed an altered alternative splicing pattern for heat shock transcription factor HsfA2 (At2g26150) in the mutant; this altered splicing is probably responsible for the increased expression of the target genes induced by HsfA2. Altered alternative splicing patterns were also detected for the transcripts of other genes in the mutant strain. These results suggest that AtSF1 has functional similarities to its yeast and metazoan counterparts.
引用
收藏
页码:591 / 603
页数:13
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