Alternatively spliced products of the human kinesin light chain 1 (KNS2) gene

被引:27
作者
McCart, AE
Mahony, D
Rothnagel, JA [1 ]
机构
[1] Univ Queensland, Dept Biochem & Mol Biol, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
关键词
alternative isoforms; alternative splicing; kinesin; kinesin light chain; multiple transcripts;
D O I
10.1034/j.1600-0854.2003.00113.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Conventional kinesin is a microtubule-based molecular motor involved in the transport of membranous and non-membranous cargoes. The kinesin holoenzyme exists as a heterotetramer, consisting of two heavy chain and two light chain subunits. It is thought that one function of the light chains is to interact with the cargo. Alternative splicing of kinesin light chain pre-mRNA has been observed in lower organisms, although evidence for alternative splicing of the human gene has not been reported. We have identified 19 variants of the human KNS2 gene (KLC1) that are generated by alternative splicing of downstream exons, but calculate that KNS2 has the potential to produce 285919 spliceforms. Corresponding spliceforms of the mouse KLC1 gene were also identified. The alternative exons are all located 3' of exon 12 and the novel spliceforms produce both alternative carboxy termini and alternative 3' untranslated regions. The observation of multiple light chain isoforms is consistent with their proposed role in specific cargo attachment.
引用
收藏
页码:576 / 580
页数:5
相关论文
共 28 条
[1]   KINESIN LIGHT-CHAINS - IDENTIFICATION AND CHARACTERIZATION OF A FAMILY OF PROTEINS FROM THE OPTIC LOBE OF THE SQUID LOLIGO-PEALII [J].
BEUSHAUSEN, S ;
KLADAKIS, A ;
JAFFE, H .
DNA AND CELL BIOLOGY, 1993, 12 (10) :901-909
[2]   A NOVEL BRAIN ATPASE WITH PROPERTIES EXPECTED FOR THE FAST AXONAL-TRANSPORT MOTOR [J].
BRADY, ST .
NATURE, 1985, 317 (6032) :73-75
[3]   CLONING AND GENETIC-CHARACTERIZATION OF THE HUMAN KINESIN LIGHT-CHAIN (KLC) GENE [J].
CABEZAARVELAIZ, Y ;
SHIH, LCN ;
HARDMAN, N ;
ASSELBERGS, F ;
BILBE, G ;
SCHMITZ, A ;
WHITE, B ;
SICILIANO, MJ ;
LACHMAN, LB .
DNA AND CELL BIOLOGY, 1993, 12 (10) :881-892
[4]   MOLECULAR-GENETICS OF KINESIN LIGHT-CHAINS - GENERATION OF ISOFORMS BY ALTERNATIVE SPLICING [J].
CYR, JL ;
PFISTER, KK ;
BLOOM, GS ;
SLAUGHTER, CA ;
BRADY, ST .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :10114-10118
[5]   The C-terminal region of the stalk domain of ubiquitous human kinesin heavy chain contains the binding site for kinesin light chain [J].
Diefenbach, RJ ;
Mackay, JP ;
Armati, PJ ;
Cunningham, AL .
BIOCHEMISTRY, 1998, 37 (47) :16663-16670
[6]   FAST AXONAL-TRANSPORT OF KINESIN IN THE RAT VISUAL-SYSTEM - FUNCTIONALITY OF KINESIN HEAVY-CHAIN ISOFORMS [J].
ELLURU, RG ;
BLOOM, GS ;
BRADY, ST .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (01) :21-40
[7]   KINESIN LIGHT-CHAIN ISOFORMS IN CAENORHABDITIS-ELEGANS [J].
FAN, J ;
AMOS, LA .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 240 (05) :507-512
[8]   Kinesin light chains are essential for axonal transport in Drosophila [J].
Gindhart, JG ;
Desai, CJ ;
Beushausen, S ;
Zinn, K ;
Goldstein, LSB .
JOURNAL OF CELL BIOLOGY, 1998, 141 (02) :443-454
[9]   Tetratrico peptide repeats are present in the kinesin light chain [J].
Gindhart, JG ;
Goldstein, LSB .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (02) :52-53
[10]  
Gyoeva FK, 2000, J CELL SCI, V113, P2047