A functional significance for codon third bases

被引:49
作者
Epstein, RJ [1 ]
Lin, K
Tan, TW
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, London, England
[2] Natl Canc Ctr, Div Med Sci, Singapore 169610, Singapore
[3] Natl Canc Ctr, Dept Med Oncol, Singapore 169610, Singapore
[4] Natl Univ Singapore, Bioinformat Ctr, Singapore, Singapore
关键词
molecular evolution;
D O I
10.1016/S0378-1119(00)00042-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Most amino acids are specified by more than one trinucleotide codon. Here we show that amino acids of differing functional importance may be distinguished by the pattern of synonymous codon usage. GC-rich genes tend to be of a greater transcriptional (p <0.01) and mitogenic (p <0.0001) significance than AT-rich genes, consistent with GC-->AT mutational drift in methylated genomic regions. Third-base GC retention also identifies critical amino acids within individual proteins, as indicated by nonrandom patterns of codon variation between gene homologs and also by differential sequelae of site-directed mutagenesis, Sequence analysis of human receptor tyrosine kinase genes confirms that functionally important transmembrane hydrophobic amino acids are specified by codons containing GC third bases more often than are transmembrane neutral amino acids (chi(2) = 134.2). Amino acids encoded by GC third bases thus appear more tightly linked to cell function and survival than are those encoded by AT third bases. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:291 / 298
页数:8
相关论文
共 29 条
[1]   A mutation at tyrosine 1062 in MEN2A-Ret and MEN2B-Ret impairs their transforming activity and association with Shc adaptor proteins [J].
Asai, N ;
Murakami, H ;
Iwashita, T ;
Takahashi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :17644-17649
[2]   UNUSUAL INSULIN BINDING TO CELLS EXPRESSING AN INSULIN-RECEPTOR MUTATED AT CYSTEINE-524 [J].
BILAN, PJ ;
YIP, CC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (03) :1891-1898
[3]   CYTOSINE METHYLATION AND THE FATE OF CPG DINUCLEOTIDES IN VERTEBRATE GENOMES [J].
COOPER, DN ;
KRAWCZAK, M .
HUMAN GENETICS, 1989, 83 (02) :181-188
[4]   MUTATIONS IN THE RET PROTOONCOGENE ARE ASSOCIATED WITH MEN 2A AND FMTC [J].
DONISKELLER, H ;
DOU, SS ;
CHI, D ;
CARLSON, KM ;
TOSHIMA, K ;
LAIRMORE, TC ;
HOWE, JR ;
MOLEY, JF ;
GOODFELLOW, P ;
WELLS, SA .
HUMAN MOLECULAR GENETICS, 1993, 2 (07) :851-856
[5]   NON-RANDOMNESS OF AMINO-ACID CHANGES IN EVOLUTION OF HOMOLOGOUS PROTEINS [J].
EPSTEIN, CJ .
NATURE, 1967, 215 (5099) :355-&
[6]   INSECT CELL-EXPRESSED P180(ERBB3) POSSESSES AN IMPAIRED TYROSINE KINASE-ACTIVITY [J].
GUY, PM ;
PLATKO, JV ;
CANTLEY, LC ;
CERIONE, RA ;
CARRAWAY, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) :8132-8136
[7]   Mutation of a src phosphorylation site in the PDGF beta-receptor leads to increased PDGF-stimulated chemotaxis but decreased mitogenesis [J].
Hansen, K ;
Johnell, M ;
Siegbahn, A ;
Rorsman, C ;
Engstrom, U ;
Wernstedt, C ;
Heldin, CH ;
Ronnstrand, L .
EMBO JOURNAL, 1996, 15 (19) :5299-5313
[8]   PDGF-INDUCED ACTIVATION OF PHOSPHOLIPASE-C IS NOT REQUIRED FOR INDUCTION OF DNA-SYNTHESIS [J].
HILL, TD ;
DEAN, NM ;
MORDAN, LJ ;
LAU, AF ;
KANEMITSU, MY ;
BOYNTON, AL .
SCIENCE, 1990, 248 (4963) :1660-1663
[9]  
Hooshmand-Rad R, 1998, J CELL SCI, V111, P607
[10]  
INUI H, 1994, J BIOL CHEM, V269, P30546