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Saccharomyces cerevisiae mutants that tolerate centromere plasmids at high copy number.

作者信息

Tschumper G, Carbon J

机构信息

Department of Biological Sciences, University of California, Santa Barbara 93106.

出版信息

Proc Natl Acad Sci U S A. 1987 Oct;84(20):7203-7. doi: 10.1073/pnas.84.20.7203.

DOI:10.1073/pnas.84.20.7203
PMID:2823253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC299258/
Abstract

Two yeast (Saccharomyces cerevisiae) mutants that tolerate centromere (CEN) plasmids at high copy number have been isolated. The mutations relieve the restraint normally imposed on plasmid copy number by a cloned CEN sequence. Our CEN plasmids specify resistance to G418 and are high copy plasmids only when the mutant host cells are grown on medium containing this antibiotic. The high copy number of the plasmids is independent of the specific cloned CEN sequence and recovered plasmids show no alteration in structure or function of the CEN DNA. The efficiency with which CEN plasmids go to high copy number is increased if the mutant cell is cotransformed by another CEN plasmid. The genomic mutation responsible for the high copy number (COP) is dominant and stable, and it segregates in a Mendelian manner. Homozygous COP/COP a/alpha diploids do not tolerate CEN plasmids at high copy number, suggesting that the mutation is regulated by mating type. The genomic DNA from both mutant cells contains an altered transposon (Ty) restriction fragment that cosegregates with the COP phenotype in crosses of mutant and wild-type strains. The mutations may be transposon-mediated events that identify a gene involved in centromere or mitotic spindle function.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/f163bb20a4be/pnas00335-0253-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/d65592b3bf04/pnas00335-0251-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/7d931bd29fa6/pnas00335-0253-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/f163bb20a4be/pnas00335-0253-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/d65592b3bf04/pnas00335-0251-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/7d931bd29fa6/pnas00335-0253-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3318/299258/f163bb20a4be/pnas00335-0253-b.jpg

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1
Saccharomyces cerevisiae mutants that tolerate centromere plasmids at high copy number.
Proc Natl Acad Sci U S A. 1987 Oct;84(20):7203-7. doi: 10.1073/pnas.84.20.7203.
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Toxic effects of excess cloned centromeres.过量克隆着丝粒的毒性作用。
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本文引用的文献

1
Temperature effects on the rate of ty transposition.温度对转座酶切的影响。
Science. 1984 Oct 5;226(4670):53-5. doi: 10.1126/science.226.4670.53.
2
Nucleotide sequence comparisons and functional analysis of yeast centromere DNAs.酵母着丝粒DNA的核苷酸序列比较与功能分析。
Cell. 1982 May;29(1):235-44. doi: 10.1016/0092-8674(82)90108-8.
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Isolation of a yeast centromere and construction of functional small circular chromosomes.酵母着丝粒的分离及功能性小环状染色体的构建。
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A yeast ribosomal DNA-binding protein that binds to the rDNA enhancer and also close to the site of Pol I transcription initiation is not important for enhancer functioning.一种与核糖体DNA(rDNA)增强子结合且也靠近RNA聚合酶I转录起始位点的酵母核糖体DNA结合蛋白,对增强子功能并不重要。
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A system for the analysis of yeast ribosomal DNA mutations.一种用于分析酵母核糖体DNA突变的系统。
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Heterogeneity and maintenance of centromere plasmid copy number in Saccharomyces cerevisiae.酿酒酵母着丝粒质粒拷贝数的异质性与维持
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Isolation of the centromere-linked CDC10 gene by complementation in yeast.通过酵母互补作用分离着丝粒连接的CDC10基因。
Proc Natl Acad Sci U S A. 1980 Apr;77(4):2173-7. doi: 10.1073/pnas.77.4.2173.
5
The yeast plasmid 2mu circle encodes components required for its high copy propagation.酵母质粒2μm环编码其高拷贝复制所需的组分。
Cell. 1983 Aug;34(1):95-104. doi: 10.1016/0092-8674(83)90139-3.
6
Copy number control by a yeast centromere.酵母着丝粒对拷贝数的控制。
Gene. 1983 Aug;23(2):221-32. doi: 10.1016/0378-1119(83)90054-9.
7
Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
J Bacteriol. 1983 Jan;153(1):163-8. doi: 10.1128/jb.153.1.163-168.1983.
8
Direct selection of Saccharomyces cerevisiae resistant to the antibiotic G418 following transformation with a DNA vector carrying the kanamycin-resistance gene of Tn903.用携带Tn903卡那霉素抗性基因的DNA载体转化后,直接筛选对抗生素G418有抗性的酿酒酵母。
Gene. 1983 Dec;26(2-3):243-52. doi: 10.1016/0378-1119(83)90194-4.
9
Structural analysis and sequence organization of yeast centromeres.酵母着丝粒的结构分析与序列组织
Cold Spring Harb Symp Quant Biol. 1983;47 Pt 2:1175-85. doi: 10.1101/sqb.1983.047.01.133.
10
Nucleotide sequence and exact localization of the neomycin phosphotransferase gene from transposon Tn5.转座子Tn5中新霉素磷酸转移酶基因的核苷酸序列及精确定位。
Gene. 1982 Oct;19(3):327-36. doi: 10.1016/0378-1119(82)90023-3.