MOLECULAR AND FUNCTIONAL-ORGANIZATION OF YEAST PLASMID-PSR1

被引:114
作者
ARAKI, H [1 ]
JEARNPIPATKUL, A [1 ]
TATSUMI, H [1 ]
SAKURAI, T [1 ]
USHIO, K [1 ]
MUTA, T [1 ]
OSHIMA, Y [1 ]
机构
[1] OSAKA UNIV, DEPT FERMENTAT TECHNOL, 2-1 YAMADAOKA, SUITA, OSAKA 565, JAPAN
关键词
D O I
10.1016/0022-2836(85)90338-9
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
The nucleotide sequence of a 6251 base-pair plasmid, pSR1, harbored in an osmophilic haploid yeast, Zygosaccharomyces rouxii (formerly Saccharomyces rouxii), was determined. No homology was detected between the sequences of pSR1 and 2 .mu.m DNA of S. cerevisiae. pSR1 has a pair of inverted repeats consisting of completely homologous 959 base-pair sequences, which separate 2 unique sequences 2654 base-pairs and 1679 base-pairs long. Each inverted repeat has an ARS sequence functional in both Z. rouxii and S. cerevisiae hosts. Short direct repeats or dyad symmetries were observed in the inverted repeats similar to those found close to the replication origin of 2-.mu.m DNA. Three open reading frames, P, S and R, each able to encode a protein of MW > 10,000, were found. Insertional inactivation of R gave rise to a defect in the intramolecular recombination at the inverted repeats, and that of S reduced the copy number of pSR1 in the S. cerevisiae host. The maintenance stability of the plasmid was also tested in the heterogeneous S. cerevisiae host, but the results of the insertional inactivation of P, S and R were ambiguous. pSR1 and 2 .mu.m DNA were compatible in S. cerevisiae cells, but the protein factors encoded by these plasmids did not complement each other.
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页码:191 / 203
页数:13
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