共 12 条
Polypyrimidine tract binding protein inhibits IgM pre-mRNA splicing by diverting U2 snRNA base- pairing away from the branch point
被引:5
|作者:
Zheng, Xuexiu
[1
]
Cho, Sunghee
[1
]
Moon, Heegyum
[1
]
Loh, Tiing Jen
[1
]
Oh, Huyn Kyung
[1
]
Green, Michael R.
[2
,3
,4
]
Shen, Haihong
[1
]
机构:
[1] Gwangju Inst Sci & Technol, Dept Life Sci, Kwangju 500712, South Korea
[2] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[4] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
来源:
基金:
新加坡国家研究基金会;
美国国家卫生研究院;
关键词:
branch point;
pre-mRNA splicing;
polypyrimidine tract binding protein;
PTB;
splicing inhibitory complex;
U2;
snRNA;
EXONS M1;
SITE;
SPLICEOSOME;
PTB;
SELECTION;
CONTACT;
STEP;
D O I:
10.1261/rna.043737.113
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 mouse immunoglobulin (IgM) pre-mRNA contains a splicing inhibitor that bears multiple binding sites for the splicing repressor polypyrimidine tract binding protein (PTB). Here we show that the inhibitor directs assembly of an ATP-dependent complex that contains PTB and U1 and U2 small nuclear RNAs (snRNAs). Unexpectedly, although U2 snRNA is present in the inhibitor complex, it is not base-paired to the branch point. We present evidence that inhibitor-bound PTB contacts U2 snRNA to promote base-pairing to an adjacent branch point-like sequence within the inhibitor, thereby preventing the U2 snRNA-branch point interaction and resulting in splicing repression. Our studies reveal a novel mechanism by which PTB represses splicing.
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页码:440 / 446
页数:7
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