NO STOP CODONS IN THE ANTISENSE STRANDS OF THE GENES FOR NYLON OLIGOMER DEGRADATION

被引:23
作者
YOMO, T [1 ]
URABE, I [1 ]
OKADA, H [1 ]
机构
[1] OSAKA UNIV,FAC ENGN,DEPT BIOTECHNOL,2-1 YAMADA OKA,SUITA,OSAKA 565,JAPAN
关键词
NEWBORN GENE; NONSTOP FRAME; GENE LIFETIME;
D O I
10.1073/pnas.89.9.3780
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
Genes for nylon oligomer-degrading enzymes are unique in the sense that the enzymes encoded by them are found not to have any appropriate substrates during most of the period of their evolution. Furthermore, these nylB genes form a family not related to any other known gene families. The base sequences of these genes were examined and a common characteristic was found: a long stretch of sequence without chain-terminating base triplets, defined as a nonstop frame (NSF), is being maintained on the antisense strand. Moreover, a certain coding frame is open for both the sense and the antisense sequences, while the other frames have many stop codons. The probability of the presence of these NSFs on the antisense strand of a gene is very small (0.0001-0.0018). In addition, another gene for nylon oligomer degradation was found to have a NSF on its antisense strand, and this gene is phylogenically independent of the nylB genes. Therefore, the presence of these NSFs is very rare and improbable. Even if the common ancestral gene of the nylB family was originally endowed with a NSF on its antisense strand, the probability of this original NSF persisting in one of its descendants of today is only 0.007. Unless an unknown force was maintaining the NSF, it would have quickly disappeared by random emergences of chain terminators. Therefore, the presence of such rare NSFs on all three antisense strands of the nylB gene family suggests that there is some special mechanism for protecting these NSFs from mutations that generate the stop codons. Such a mechanism may enable NSFs to evolve into new functional genes and hence seems to be a basic mechanism for the birth of new enzymes.
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页码:3780 / 3784
页数:5
相关论文
共 21 条
[1]   2 MAMMALIAN GENES TRANSCRIBED FROM OPPOSITE STRANDS OF THE SAME DNA LOCUS [J].
ADELMAN, JP ;
BOND, CT ;
DOUGLASS, J ;
HERBERT, E .
SCIENCE, 1987, 235 (4795) :1514-1517
[2]   CODON USAGE TABULATED FROM THE GENBANK GENETIC SEQUENCE DATA [J].
AOTA, S ;
GOJOBORI, T ;
ISHIBASHI, F ;
MARUYAMA, T ;
IKEMURA, T .
NUCLEIC ACIDS RESEARCH, 1988, 16 :R315-R402
[3]   COMPLEMENTARITY OF PEPTIDES SPECIFIED BY SENSE AND ANTISENSE STRANDS OF DNA [J].
BLALOCK, JE .
TRENDS IN BIOTECHNOLOGY, 1990, 8 (06) :140-144
[4]  
Dayhoff MO., 1978, ATLAS PROTEIN SEQ ST, V5, P345
[5]   PLASMID DEPENDENCE OF PSEUDOMONAS SP STRAIN NK87 ENZYMES THAT DEGRADE 6-AMINOHEXANOATE-CYCLIC DIMER [J].
KANAGAWA, K ;
NEGORO, S ;
TAKADA, N ;
OKADA, H .
JOURNAL OF BACTERIOLOGY, 1989, 171 (06) :3181-3186
[6]  
Kimura M., 1983, NEUTRAL THEORY MOL E
[7]   PURIFICATION AND CHARACTERIZATION OF 6-AMINOHEXANOIC-ACID-OLIGOMER HYDROLASE OF FLAVOBACTERIUM SP-KI72 [J].
KINOSHITA, S ;
TERADA, T ;
TANIGUCHI, T ;
TAKENE, Y ;
MASUDA, S ;
MATSUNAGA, N ;
OKADA, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1981, 116 (03) :547-551
[8]   6-AMINOHEXANOIC ACID CYCLIC DIMER HYDROLASE - NEW CYCLIC AMIDE HYDROLASE PRODUCED BY ACROMOBACTER-GUTTATUS KI72 [J].
KINOSHITA, S ;
NEGORO, S ;
MURAMATSU, M ;
BISARIA, VS ;
SAWADA, S ;
OKADA, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1977, 80 (02) :489-495
[9]   UTILIZATION OF A CYCLIC DIMER AND LINEAR OLIGOMERS OF EPSILON-AMINOCAPROIC ACID BY ACHROMOBACTER-GUTTATUS KI-72 [J].
KINOSHITA, S ;
KAGEYAMA, S ;
IBA, K ;
YAMADA, Y ;
OKADA, H .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1975, 39 (06) :1219-1223
[10]   2 ERBA HOMOLOGS ENCODING PROTEINS WITH DIFFERENT T3 BINDING-CAPACITIES ARE TRANSCRIBED FROM OPPOSITE DNA STRANDS OF THE SAME GENETIC-LOCUS [J].
MIYAJIMA, N ;
HORIUCHI, R ;
SHIBUYA, Y ;
FUKUSHIGE, S ;
MATSUBARA, K ;
TOYOSHIMA, K ;
YAMAMOTO, T .
CELL, 1989, 57 (01) :31-39