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第四条染色体上七个开放阅读框的破坏与功能分析:YDL057w、YDL012c、YDL010w、YDL009c、YDL008w(APC11)、YDL005c(MED2)和YDL003w(MCD1)。

Disruption and functional analysis of seven ORFs on chromosome IV: YDL057w, YDL012c, YDL010w, YDL009c, YDL008w (APC11), YDL005c (MED2) and YDL003w (MCD1).

作者信息

Smith K N, Iwanejko L, Loeillet S, Fabre F, Nicolas A

机构信息

Institut Curie, Section de Recherche, CNRS UMR 144, 26, Rue d'Ulm, 75248 Paris Cedex 05, France.

出版信息

Yeast. 1999 Sep 15;15(12):1255-67. doi: 10.1002/(SICI)1097-0061(19990915)15:12<1255::AID-YEA451>3.0.CO;2-L.

Abstract

In the context of the EUROFAN project, we have carried out the systematic disruption of seven ORFs on chromosome IV of Saccharomyces cerevisiae using the long flanking homology technique to replace each ORF with the KanMX cassette. Targeted disruption of YDL057w, YDL012c, or YDL010w with YDL009c (the two ORFs overlap) confers no overt defects in haploid growth on a variety of media at different temperatures, in mating, or in the sporulation of diploids homozygous for the disruption. By contrast, YDL008w and YDL003w disruptants are non-viable. The product of YDL008w (elsewhere identified as APC11) is a component of the anaphase promoting complex. YDL003w (also termed MCD1) is a homologue of Schizosaccharomyces pombe rad21, an essential gene implicated in DNA double-strand break repair and nuclear organization in fission yeast. In budding yeast, this ORF has been shown by several laboratories to encode a protein involved in sister chromatid cohesion and chromosome condensation. The remaining ORF, YDL005c (also termed MED2), encodes a component of the transcriptional activator complex known as Mediator. Disruption of YDL005c confers a modest slow growth phenotype on rich medium and a more severe phenotype on minimal medium, aberrant cellular morphology, and mating defects; diploids homozygous for the disruption cannot sporulate.

摘要

在EUROFAN项目的背景下,我们利用长侧翼同源技术对酿酒酵母IV号染色体上的7个开放阅读框(ORF)进行了系统性破坏,用KanMX盒取代每个ORF。用YDL009c(这两个ORF重叠)对YDL057w、YDL012c或YDL010w进行靶向破坏,在不同温度下的各种培养基上的单倍体生长、交配或破坏纯合二倍体的孢子形成过程中,均未表现出明显缺陷。相比之下,YDL008w和YDL003w破坏株无法存活。YDL008w的产物(在其他地方被鉴定为APC11)是后期促进复合物的一个组成部分。YDL003w(也称为MCD1)是粟酒裂殖酵母rad21的同源物,rad21是一个与裂殖酵母DNA双链断裂修复和核组织有关的必需基因。在芽殖酵母中,几个实验室已证明这个ORF编码一种参与姐妹染色单体黏连和染色体凝聚的蛋白质。其余的ORF,YDL005c(也称为MED2),编码一种称为中介体的转录激活复合物的组成部分。YDL005c的破坏在丰富培养基上导致适度的生长缓慢表型,在基本培养基上导致更严重的表型、异常的细胞形态和交配缺陷;破坏纯合的二倍体无法形成孢子。

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