Ntc90 is required for recruiting first step factor Yju2 but not for spliceosome activation

被引:15
作者
Chang, Kae-Jiun [1 ,2 ]
Chen, Hsin-Chou [1 ,2 ]
Cheng, Soo-Chen [1 ,2 ]
机构
[1] Acad Sinica, Inst Mol Biol, Taipei 115, Taiwan
[2] Natl Yang Ming Univ, Inst Microbiol & Immunol, Taipei 112, Taiwan
关键词
first catalytic reaction; Ntc90; RNA splicing; splicing reaction; PRE-MESSENGER-RNA; CELL-CYCLE PROGRESSION; PRP19P-ASSOCIATED COMPLEX; SACCHAROMYCES-CEREVISIAE; SPLICING FACTORS; PRP19-ASSOCIATED COMPLEX; PHYSICAL INTERACTIONS; PROTEIN; COMPONENTS; PRP2;
D O I
10.1261/rna.1625309
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 Prp19-associated complex (NineTeen Complex [NTC]) is required for spliceosome activation by specifying interactions of U5 and U6 with pre-mRNA on the spliceosome after the release of U4. The NTC consists of at least eight protein components, including two tetratricopeptide repeat (TPR)-containing proteins, Ntc90 and Ntc77. Ntc90 has nine copies of the TPR with seven clustered in the carboxy-terminal half of the protein, and interacts with all identified NTC components except for Prp19 and Ntc25. It forms a stable complex with Ntc31, Ntc30, and Ntc20 in the absence of Ntc25, when other interactions between NTC components are disrupted. In this study, we used both biochemical and genetic methods to analyze the structure of Ntc90, and its function in maintaining the integrity of the NTC and in NTC-mediated spliceosome activation. Our results show that Ntc90 interacts with Ntc31, Ntc30, and other NTC components through different regions of the protein, and that its function may be regulated by Ntc31 and Ntc30. Ntc90 is not required for the association of Prp19, Ntc85, Ntc77, Ntc25, and Ntc20, or for their binding to the spliceosome. It is also not required for NTC-mediated spliceosome activation, but is required for the recruitment of Yju2, which is involved in the first catalytic reaction after the function of Prp2. Our results demonstrate a novel role of the NTC in recruiting splicing factors to the spliceosome after its activation.
引用
收藏
页码:1729 / 1739
页数:11
相关论文
共 31 条
[1]   Identification and characterization of Prp45p and Prp46p, essential pre-mRNA splicing factors [J].
Albers, M ;
Diment, A ;
Muraru, M ;
Russell, CS ;
Beggs, JD .
RNA, 2003, 9 (01) :138-150
[2]  
Ben-Yehuda S, 2000, GENETICS, V156, P1503
[3]  
BURGE CB, 1999, RNA WORLD 2
[4]   The Prp19-associated complex is required for specifying interactions of U5 and U6 with pre-mRNA during spliceosome activation [J].
Chan, SP ;
Cheng, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (35) :31190-31199
[5]   The Prp19p-associated complex in spliceosome activation [J].
Chan, SP ;
Kao, DI ;
Tsai, WY ;
Cheng, SC .
SCIENCE, 2003, 302 (5643) :279-282
[6]   Functional links between the Prp19-associated complex, U4/U6 biogenesis, and spliceosome recycling [J].
Chen, CH ;
Kao, DI ;
Chan, SP ;
Kao, TC ;
Lin, JY ;
Cheng, SC .
RNA, 2006, 12 (05) :765-774
[7]   Functional and physical interactions between components of the Prp19p-associated complex [J].
Chen, CH ;
Yu, WC ;
Tsao, TY ;
Wang, LY ;
Chen, HR ;
Lin, JY ;
Tsai, WY ;
Cheng, SC .
NUCLEIC ACIDS RESEARCH, 2002, 30 (04) :1029-1037
[8]   Identification and characterization of two novel components of the prp19p-associated complex, Ntc30p and Ntc20p [J].
Chen, CH ;
Tsai, WY ;
Chen, HR ;
Wang, CH ;
Cheng, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (01) :488-494
[9]   Snt309p modulates interactions of Prp19p with its associated components to stabilize the Prp19p-associated complex essential for pre-mRNA splicing [J].
Chen, HR ;
Tsao, TY ;
Chen, CH ;
Tsai, WY ;
Her, LS ;
Hsu, MMT ;
Cheng, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5406-5411
[10]   Snt309p, a component of the Prp19p-associated complex that interacts with Prp19p and associates with the spliceosome simultaneously with or immediately after dissociation of U4 in the same manner as Prp19p [J].
Chen, HR ;
Jan, SP ;
Tsao, TY ;
Sheu, YJ ;
Banroques, J ;
Cheng, SC .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :2196-2204