Cross-intron bridging interactions in the yeast commitment complex are conserved in mammals

被引:290
作者
Abovich, N [1 ]
Rosbash, M [1 ]
机构
[1] BRANDEIS UNIV, HOWARD HUGHES MED INST, DEPT BIOL, WALTHAM, MA 02254 USA
关键词
D O I
10.1016/S0092-8674(00)80221-4
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 commitment complex is the first defined step in the yeast (S. cerevisiae) splicing pathway. It contains U1 snRNP as well as Mud2p, which resembles human U2AF65. In a genetic screen, we identified the yeast gene MSL-5, which is a novel commitment complex component. Genetic and biochemical criteria indicate a direct interaction between MsI5p and both Mud2p and the U1 snRNP protein Prp40p. This defines a bridge between the two ends of the intron. MsI5p (renamed BBP for branchpoint bridging protein) has a mammalian ortholog, the splicing factor SF1. Our results show that SF1 interacts strongly with human U2AF65, and that SF1 is a bona fide E complex component. This implies that aspects of these novel cross-intron protein-protein interactions are conserved between yeast and mammals.
引用
收藏
页码:403 / 412
页数:10
相关论文
共 55 条
[1]   THE YEAST MUD2 PROTEIN - AN INTERACTION WITH PRP11 DEFINES A BRIDGE BETWEEN COMMITMENT COMPLEXES AND U2 SNRNP ADDITION [J].
ABOVICH, N ;
LIAO, XLC ;
ROSBASH, M .
GENES & DEVELOPMENT, 1994, 8 (07) :843-854
[2]  
Arning S, 1996, RNA, V2, P794
[3]   A U1/U4/U5 snRNP complex induced by a 2'-O-methyl-oligoribonucleotide complementary to U5 snRNA [J].
Ast, G ;
Weiner, AM .
SCIENCE, 1996, 272 (5263) :881-884
[4]  
BEDFORD MT, 1997, IN PRESS EMBO J
[5]   GENETIC AND PHYSICAL INTERACTIONS BETWEEN SRP1P AND NUCLEAR-PORE COMPLEX PROTEINS NUP1P AND NUP2P [J].
BELANGER, KD ;
KENNA, MA ;
WEI, S ;
DAVIS, LI .
JOURNAL OF CELL BIOLOGY, 1994, 126 (03) :619-630
[6]   PROTEIN-COMPONENTS SPECIFICALLY ASSOCIATED WITH PRESPLICEOSOME AND SPLICEOSOME COMPLEXES [J].
BENNETT, M ;
MICHAUD, S ;
KINGSTON, J ;
REED, R .
GENES & DEVELOPMENT, 1992, 6 (10) :1986-2000
[7]   THE WW DOMAIN - A SIGNALING SITE IN DYSTROPHIN [J].
BORK, P ;
SUDOL, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (12) :531-533
[8]   Formin binding proteins bear WWP/WW domains that bind proline-rich peptides and functionally resemble SH3 domains [J].
Chan, DC ;
Bedford, MT ;
Leder, P .
EMBO JOURNAL, 1996, 15 (05) :1045-1054
[9]   THE WW DOMAIN OF YES-ASSOCIATED PROTEIN BINDS A PROLINE-RICH LIGAND THAT DIFFERS FROM THE CONSENSUS ESTABLISHED FOR SRC HOMOLOGY 3-BINDING MODULES [J].
CHEN, HI ;
SUDOL, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7819-7823
[10]   FIRST GLIMPSES AT STRUCTURE-FUNCTION-RELATIONSHIPS OF THE NUCLEOCAPSID PROTEIN OF RETROVIRUSES [J].
DARLIX, JL ;
LAPADATTAPOLSKY, M ;
DEROCQUIGNY, H ;
ROQUES, BP .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 254 (04) :523-537