HUMAN NONMUSCLE MYOSIN HEAVY-CHAIN MESSENGER-RNA - GENERATION OF DIVERSITY THROUGH ALTERNATIVE POLYADENYLYLATION

被引:129
作者
SAEZ, CG
MYERS, JC
SHOWS, TB
LEINWAND, LA
机构
[1] NEW YORK STATE DEPT HLTH,ROSWELL PK MEM INST,DEPT HUMAN GENET,BUFFALO,NY 14263
[2] UNIV PENN,SCH MED,DEPT BIOCHEM & BIOPHYS,PHILADELPHIA,PA 19104
关键词
Chromosome mapping; DNA sequence;
D O I
10.1073/pnas.87.3.1164
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
Myosin is a ubiquitous eukaryotic contractile protein that generates the force responsible for such diverse cellular movements as muscle contraction and cytokinesis. Although there have been numerous studies of sarcomeric myosin heavy chain (MHC) genes, no molecular clones have been reported that encode mammalian nonmuscle MHC. This study presents the molecular genetic characterization of a human nonmuscle MHC that is expressed in fibroblasts, endothelial cells, and macrophages. Human nonmuscle MHC amino acids are weakly homologous (33%) to sarcomeric MHC but are -72% identical to smooth muscle MHC. In contrast to vertebrate sarcomeric MHCs, which generate diversity through the expression of members of a multigene family, an alternative polyadenylylation site is used in the nonmuscle MHC gene to generate multiple transcripts that encode the same protein. We have mapped this gene to chromosome 22. It is thus unlinked to either of the sarcomeric MHC gene clusters on human chromosomes 14 and 17.
引用
收藏
页码:1164 / 1168
页数:5
相关论文
共 36 条
[1]   SIZING AND MAPPING OF EARLY ADENOVIRUS MESSENGER-RNAS BY GEL-ELECTROPHORESIS OF S1 ENDONUCLEASE-DIGESTED HYBRIDS [J].
BERK, AJ ;
SHARP, PA .
CELL, 1977, 12 (03) :721-732
[2]   ALTERNATIVE SPLICING - A UBIQUITOUS MECHANISM FOR THE GENERATION OF MULTIPLE PROTEIN ISOFORMS FROM SINGLE GENES [J].
BREITBART, RE ;
ANDREADIS, A ;
NADALGINARD, B .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :467-495
[3]   PURIFICATION AND STRUCTURAL-ANALYSIS OF MYOSINS FROM BRAIN AND OTHER NON-MUSCLE TISSUES [J].
BURRIDGE, K ;
BRAY, D .
JOURNAL OF MOLECULAR BIOLOGY, 1975, 99 (01) :1-&
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]   REGULATION OF NONMUSCLE MYOSIN STRUCTURE AND FUNCTION [J].
CITI, S ;
KENDRICKJONES, J .
BIOESSAYS, 1987, 7 (04) :155-159
[6]   DISRUPTION OF THE DICTYOSTELIUM MYOSIN HEAVY-CHAIN GENE BY HOMOLOGOUS RECOMBINATION [J].
DELOZANNE, A ;
SPUDICH, JA .
SCIENCE, 1987, 236 (4805) :1086-1091
[7]   MOLECULAR-GENETICS OF MYOSIN [J].
EMERSON, CP ;
BERNSTEIN, SI .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :695-726
[8]   HUMAN CYTOPLASMIC ACTIN PROTEINS ARE ENCODED BY A MULTIGENE FAMILY [J].
ENGEL, J ;
GUNNING, P ;
KEDES, L .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (06) :674-684
[9]   MOLECULAR-CLONING OF A GENE SELECTIVELY INDUCED BY GAMMA INTERFERON FROM HUMAN MACROPHAGE CELL-LINE U937 [J].
FAN, XD ;
STARK, GR ;
BLOOM, BR .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (05) :1922-1928
[10]   MOLECULAR GENETIC-CHARACTERIZATION OF A DEVELOPMENTALLY REGULATED HUMAN PERINATAL MYOSIN HEAVY-CHAIN [J].
FEGHALI, R ;
LEINWAND, LA .
JOURNAL OF CELL BIOLOGY, 1989, 108 (05) :1791-1797