Elucidating sequence codes: Three codes for evolution

被引:53
作者
Trifonov, EN [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Struct, IL-76100 Rehovot, Israel
来源
MOLECULAR STRATEGIES IN BIOLOGICAL EVOLUTION | 1999年 / 870卷
关键词
D O I
10.1111/j.1749-6632.1999.tb08894.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The sequences are related to evolution in several ways. First, they carry traces of a distant past. Two sequence features point to the earliest sequence organization. The universal hidden GCU-periodical pattern in mRNA suggests the earliest codons: GCU and its nine-point-change derivatives. They code for seven amino acids that by several criteria are also the oldest. Together it makes the earliest form of the triplet code, still recognizable in the extant sequences. Another feature present in the sequences, apparently, since separation of prokaryotes and eukaryotes, is hidden genome segmentation. Both protein coding and noncoding sequences appear to have been formed by fusion of standard size units, about 360 bp (120 aa) in eukaryotes and 450 bp (150 aa) in prokaryotes. Presumably, the units have been functioning at some stage of evolution as autonomous single gene size elements. There are sequence designs that promote evolution. One such design suitable for fast adaptation is the tandem repetition of identical sequences, so that their copy numbers in the repeat arrays would modulate (tune) the expression of nearby genes. The tandem repeat expansion diseases illustrate this mechanism in a dramatic way: overtuning of the respective gene expression leads to the disease.
引用
收藏
页码:330 / 338
页数:9
相关论文
共 40 条
[1]   A complementary circular code in the protein coding genes [J].
Arques, DG ;
Michel, CJ .
JOURNAL OF THEORETICAL BIOLOGY, 1996, 182 (01) :45-58
[2]   Trinucleotide repeat expansion and human disease [J].
Ashley, CT ;
Warren, ST .
ANNUAL REVIEW OF GENETICS, 1995, 29 :703-728
[3]  
Baev A S, 1972, Mol Biol, V6, P612
[4]   SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS [J].
BENNETT, ST ;
LUCASSEN, AM ;
GOUGH, SCL ;
POWELL, EE ;
UNDLIEN, DE ;
PRITCHARD, LE ;
MERRIMAN, ME ;
KAWAGUCHI, Y ;
DRONSFIELD, MJ ;
POCIOT, F ;
NERUP, J ;
BOUZEKRI, N ;
CAMBONTHOMSEN, A ;
RONNINGEN, KS ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE GENETICS, 1995, 9 (03) :284-292
[5]   UNDERLYING ORDER IN PROTEIN-SEQUENCE ORGANIZATION [J].
BERMAN, AL ;
KOLKER, E ;
TRIFONOV, EN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :4044-4047
[6]   Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation [J].
Cochran, EJ ;
Bennett, DA ;
Cervenakova, L ;
Kenney, K ;
Bernard, B ;
Foster, NL ;
Benson, DF ;
Goldfarb, LG ;
Brown, P .
NEUROLOGY, 1996, 47 (03) :727-733
[7]   HYPERCYCLE - PRINCIPLE OF NATURAL SELF-ORGANIZATION .C. REALISTIC HYPERCYCLE [J].
EIGEN, M ;
SCHUSTER, P .
NATURWISSENSCHAFTEN, 1978, 65 (07) :341-369
[8]   TRANSFER-RNA, AN EARLY GENE [J].
EIGEN, M ;
WINKLEROSWATITSCH, R .
NATURWISSENSCHAFTEN, 1981, 68 (06) :282-292
[9]   TRANSFER-RNA - THE EARLY ADAPTER [J].
EIGEN, M ;
WINKLEROSWATITSCH, R .
NATURWISSENSCHAFTEN, 1981, 68 (05) :217-228
[10]   ENHANCED GENE-EXPRESSION BY THE POLY(DT-DG) . POLY(DC-DA) SEQUENCE [J].
HAMADA, H ;
SEIDMAN, M ;
HOWARD, BH ;
GORMAN, CM .
MOLECULAR AND CELLULAR BIOLOGY, 1984, 4 (12) :2622-2630