COMPLETE DNA-SEQUENCE OF YEAST CHROMOSOME-II

被引:205
作者
FELDMANN, H
AIGLE, M
ALJINOVIC, G
ANDRE, B
BACLET, MC
BARTHE, C
BAUR, A
BECAM, AM
BITEAU, N
BOLES, E
BRANDT, T
BRENDEL, M
BRUCKNER, M
BUSSEREAU, F
CHRISTIANSEN, C
CONTRERAS, R
CROUZET, M
CZIEPLUCH, C
DEMOLIS, N
DELAVEAU, T
DOIGNON, F
DOMDEY, H
DUSTERHUS, S
DUBOIS, E
DUJON, B
ELBAKKOURY, M
ENTIAN, KD
FEUERMANN, M
FIERS, W
FOBO, GM
FRITZ, C
GASSENHUBER, H
GLANSDORFF, N
GOFFEAU, A
GRIVELL, LA
DEHAAN, M
HEIN, C
HERBERT, CJ
HOLLENBERG, CP
HOLMSTROM, K
JACQ, C
JACQUET, M
JAUNIAUX, JC
JONNIAUX, JL
KALLESOE, T
KIESAU, P
KIRCHRATH, L
KOTTER, P
KOROLL, S
LIEBL, S
机构
[1] UNIV BORDEAUX 2,BIOL MOLEC & SEQUENCAGE LAB,F-33076 BORDEAUX,FRANCE
[2] GESELL ANAL TECHN & CONSULTING,D-78467 CONSTANCE,GERMANY
[3] FREE UNIV BRUSSELS,PHYSIOL CELLULAIRE & GENET LEVURES,B-1050 BRUSSELS,BELGIUM
[4] TH DARMSTADT,INST MIKROBIOL,D-64287 DARMSTADT,GERMANY
[5] CNRS,CTR GENET MOLEC,F-91198 GIF SUR YVETTE,FRANCE
[6] BIOTECHNOL INST,AGROIND TECHNOL & MOLEC BIOTECHNOL,FOOD TECHNOL RES INST,DK-2800 LYNGBY,DENMARK
[7] UNIV FRANKFURT,INST MIKROBIOL,D-60596 FRANKFURT,GERMANY
[8] GENOTYPE GMBH,BIOTECHNOL & MOLEK BIOL FORSCH,D-69295 WILHELMSFELD,GERMANY
[9] UNIV PARIS 11,INST GENET MICROBIOL,INFORMAT GENET & DEV,CNRS,URA 1354,F-91405 ORSAY,FRANCE
[10] STATE UNIV GHENT,MOLEC BIOL LAB,B-9000 GHENT,BELGIUM
[11] DEUTSCH KREBSFORSCHUNGSZENTRUM,INSERM,U375,D-69009 HEIDELBERG,GERMANY
[12] ECOLE NORMALE SUPER,MOLEC GENET LAB,CNRS,URA 1302,F-75230 PARIS 05,FRANCE
[13] UNIV MUNICH,GENZENTRUM,MOLEK BIOL LAB,D-82152 MARTINSRIED,GERMANY
[14] UNIV FRANKFURT,BIOZENTRUM,INST MIKROBIOL,D-60439 FRANKFURT,GERMANY
[15] FREE UNIV BRUSSELS,INST RECH CERIA,COOVI,MICROBIOL LAB,B-1070 BRUSSELS,BELGIUM
[16] FREE UNIV BRUSSELS,ERFELKHEIDESLEER MICROBIOL LAB,B-1070 BRUSSELS,BELGIUM
[17] INST PASTEUR,DEPT BIOL MOLEC,UNITE GENET MOLEC LEVURES,CNRS,URA 1149,F-75724 PARIS 15,FRANCE
[18] UNIV STRASBOURG 1,CNRS,INST BOT,F-67083 STRASBOURG,FRANCE
[19] MAX PLANCK INST BIOCHEM,MIPS,D-82152 MARTINSRIED,GERMANY
[20] UNIV DUSSELDORF,INST MIKROBIOL,D-40225 DUSSELDORF,GERMANY
[21] UNIV CATHOLIQUE LOUVAIN,UNITE BIOCHIM PHYSIOL,B-1348 LOUVAIN,BELGIUM
[22] COMMISS EUROPEAN COMMUNITIES,B-1049 BRUSSELS,BELGIUM
[23] UNIV AMSTERDAM,MOLEC BIOL SECT,VAKGRP MOLEC CELBIOL,1098 SM AMSTERDAM,NETHERLANDS
[24] UNIV DUBLIN TRINITY COLL,DEPT GENET,DUBLIN 2,IRELAND
[25] JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
[26] UNIV KONSTANZ,FAK BIOL,D-78434 CONSTANCE,GERMANY
[27] LEIDEN UNIV,DEPT CELL BIOL & GENET,CLUSIUS LAB,2333 AL LEIDEN,NETHERLANDS
关键词
COMPOSITIONAL BIAS; GENE FUNCTION; GENE REDUNDANCY; GENOME ORGANIZATION; PUTATIVE REPLICATION ORIGINS;
D O I
10.1002/j.1460-2075.1994.tb06923.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the framework of the EU genome-sequencing programmes, the complete DNA sequence of the yeast Saccharomyces cerevisiae chromosome II (807 188 bp) has been determined. At present, this is the largest eukaryotic chromosome entirely sequenced. A total of 410 open reading frames (ORFs) were identified, covering 72% of the sequence. Similarity searches revealed that 124 ORFs (30%) correspond to genes of known function, 51 ORFs (12.5%) appear to be homologues of genes whose functions are known, 52 others (12.5 %) have homologues the functions of which are not well defined and another 33 of the novel putative genes (8%) exhibit a degree of similarity which is insufficient to confidently assign function. Of the genes on chromosome II, 37-45% are thus of unpredicted function. Among the novel putative genes, we found several that are related to genes that perform differentiated functions in multicellular organisms or are involved in malignancy. In addition to a compact arrangement of potential protein coding sequences, the analysis of this chromosome confirmed general chromosome patterns but also revealed particular novel features of chromosomal organization, Alternating regional variations in average base composition correlate with variations in local gene density along chromosome II, as observed in chromosomes XI and III. We propose that functional ARS elements are preferably located in the AT-rich regions that have a spacing of similar to-110 kb, Similarly, the 13 tRNA genes and the three Ty elements of chromosome II are found in AT-rich regions, In chromosome II, the distribution of coding sequences between the two strands is biased, with a ratio of 1.3:1, An interesting aspect regarding the evolution of the eukaryotic genome is the finding that chromosome II has a high degree of internal genetic redundancy, amounting to 16% of the coding capacity.
引用
收藏
页码:5795 / 5809
页数:15
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