Identification of both shared and distinct proteins in the major and minor spliceosomes

被引:106
作者
Will, CL
Schneider, C
Reed, R
Lührmann, R
机构
[1] Univ Marburg, Inst Mol Biol & Tumorforsch, D-35037 Marburg, Germany
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[3] Max Planck Inst Biophys Chem, Dept Cellular Biochem, D-37070 Gottingen, Germany
关键词
D O I
10.1126/science.284.5422.2003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In metazoa ns, two distinct spliceosomes catalyzing pre-messenger RNA splicing have been identified. Here, the human U11/U12 small nuclear ribonucleoprotein (snRNP), a subunit of the minor (U12-dependent) spliceosome, was isolated. Twenty U11/U72 proteins were identified, including subsets unique to the minor spliceosome or common to both spliceosomes. Common proteins include four U2 snRNP polypeptides that constitute the essential splicing factor SF3b. A 35-kilodalton U11-associated protein homologous to the U1 snRNP 70K protein was also identified. These data provide fundamental information about proteins of the minor spliceosome and shed light on its evolutionary relationship to the major spliceosome.
引用
收藏
页码:2003 / 2005
页数:3
相关论文
共 30 条
[1]   Cross-intron bridging interactions in the yeast commitment complex are conserved in mammals [J].
Abovich, N ;
Rosbash, M .
CELL, 1997, 89 (03) :403-412
[2]  
[Anonymous], UNPUB
[3]   WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: The proline glycine and methionine-rich motif [J].
Bedford, MT ;
Reed, R ;
Leder, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10602-10607
[4]   SMALL NUCLEAR RIBONUCLEOPROTEIN (RNP)-U2 CONTAINS NUMEROUS ADDITIONAL PROTEINS AND HAS A BIPARTITE RNP STRUCTURE UNDER SPLICING CONDITIONS [J].
BEHRENS, SE ;
TYC, K ;
KASTNER, B ;
REICHELT, J ;
LUHRMANN, R .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) :307-319
[5]   The splicing factor BBP interacts specifically with the pre-mRNA branchpoint sequence UACUAAC [J].
Berglund, JA ;
Chua, K ;
Abovich, N ;
Reed, R ;
Rosbash, M .
CELL, 1997, 89 (05) :781-787
[6]   Evolutionary fates and origins of U12-type introns [J].
Burge, CB ;
Padgett, RA ;
Sharp, PA .
MOLECULAR CELL, 1998, 2 (06) :773-785
[7]  
Burge CB, 1999, RNA WORLD, P525
[8]   THE PRESPLICEOSOME COMPONENTS SAP-49 AND SAP-145 INTERACT IN A COMPLEX IMPLICATED IN TETHERING U2-SNRNP TO THE BRANCH SITE [J].
CHAMPIONARNAUD, P ;
REED, R .
GENES & DEVELOPMENT, 1994, 8 (16) :1974-1983
[9]   Initial recognition of U12-dependent introns requires both U11/5′ splice-side and U12/branchpoint interactions [J].
Frilander, MJ ;
Steitz, JA .
GENES & DEVELOPMENT, 1999, 13 (07) :851-863
[10]   Evidence that sequence-independent binding of highly conserved U2 snRNP proteins upstream of the branch site is required for assembly of spliceosomal complex A [J].
Gozani, O ;
Feld, R ;
Reed, R .
GENES & DEVELOPMENT, 1996, 10 (02) :233-243