Cloning, expression, and complementation test of the RNA lariat debranching enzyme cDNA from mouse

被引:1
|
作者
Kim, HC
Kim, GM
Yang, JM
Kim, JW [1 ]
机构
[1] Inha Univ, Inha Res Inst Med Sci, Inchon 402751, South Korea
[2] Inha Univ, Coll Med, Dept Biochem, Inchon 402751, South Korea
[3] Samsung Biomed Res Inst, Clin Res Ctr, Seoul 135230, South Korea
[4] Sungkyunkwan Univ, Sch Med, Dept Dermatol, Seoul 135230, South Korea
关键词
complementation; intron accumulation; mouse; RNA lariat debranching enzyme; Saccharomyces cerevisiae;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The RNA lariat debranching enzyme of mouse (mDBR1) was cloned by screening a NIH/3T3 cDNA library. The sequence of full-length mDBR1 cDNA contained a single 515 amino acid open reading frame of 58 kDa protein, Comparison of the amino acid sequence of mDBR1 to other DBR proteins showed 40%, 44%, 43%, 42%, and 80% identity to Saccharomyces cerevisiae, Schizosaccharomyces pombe, Caenorhabditis elegans, Drosophila melanogaster, and human debranching enzymes, respectively, The mDBR1 cDNA was shown to be functional in an interspecies specific complementation experiment, and an in vitro debranching enzyme assay. Mouse DBR1 could complement the intron accumulation phenotype of a S, cerevisiae dbr1 null mutant strain. However, the level of complementation depended on the copy number of the mDBR1 cDNA, The integration of the mDBR1 cDNA in the chromosome of S, pombe also complemented both intron accumulation and slow growth phenotypes of the S, pombe dbr1 knock-out mutant strain.
引用
收藏
页码:198 / 203
页数:6
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