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酿酒酵母的一系列实验室菌株携带涉及染色体I和III的重排。

A family of laboratory strains of Saccharomyces cerevisiae carry rearrangements involving chromosomes I and III.

作者信息

Casaregola S, Nguyen H V, Lepingle A, Brignon P, Gendre F, Gaillardin C

机构信息

Collection de Levures d'Intérêt Biotechnologique, Laboratoire de Génétique Moléculaire et Cellulaire, INRA/CNRS, INA-PG, Thiverval-Grignon, France.

出版信息

Yeast. 1998 Apr 30;14(6):551-64. doi: 10.1002/(SICI)1097-0061(19980430)14:6<551::AID-YEA260>3.0.CO;2-Q.

Abstract

In order to study meiotic segregation of chromosome length polymorphism in yeast, we analysed the progeny of a cross involving two laboratory strains FL100trp and YNN295. Analysis of the parental strains led us to detect an important length polymorphism of chromosomes I and III in FL100trp. A reciprocal translocation involving 80 kb of the left arm of chromosome III and 45 kb of the right arm of chromosome I was shown to be the cause for the observed polymorphism in this strain. The characterization of the translocation breakpoints revealed the existence of a transposition hot-spot on chromosome I: the sequence of the translocation joints on chromosomes I and III suggests that the mechanism very likely involved homologous recombination between Ty2 transposable elements on each chromosome. Analysis of FL100, FL200 and FL100trp ura, which are related to FL100trp, shows that this reciprocal translocation is present in some of the strains of the FL series, whereas the parental strain FL100 does not carry the same rearrangement. We evidenced instead the duplication of 80 kb of chromosome III on chromosome I and a deletion of 45 kb of the right arm of chromosome I in this strain, indicating that secondary events might have taken place and that the strain currently named FL100 is not the common ancestor of the FL series.

摘要

为了研究酵母中染色体长度多态性的减数分裂分离,我们分析了涉及两个实验室菌株FL100trp和YNN295的杂交后代。对亲本菌株的分析使我们检测到FL100trp中染色体I和III的重要长度多态性。涉及染色体III左臂80 kb和染色体I右臂45 kb的相互易位被证明是该菌株中观察到的多态性的原因。易位断点的表征揭示了染色体I上存在一个转座热点:染色体I和III上易位接头的序列表明,该机制很可能涉及每条染色体上Ty2转座元件之间的同源重组。对与FL100trp相关的FL100、FL200和FL100trp ura的分析表明,这种相互易位存在于FL系列的一些菌株中,而亲本菌株FL100不携带相同的重排。相反,我们证明了该菌株中染色体I上有80 kb的染色体III重复,染色体I右臂有45 kb的缺失,这表明可能发生了二次事件,并且目前命名为FL100的菌株不是FL系列的共同祖先。

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