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剖析酿酒酵母中的pet18突变:HTL1编码一种与RSC复合体组分相互作用的7 kDa多肽。

Dissecting the pet18 mutation in Saccharomyces cerevisiae: HTL1 encodes a 7-kDa polypeptide that interacts with components of the RSC complex.

作者信息

Lu Y-M, Lin Y-R, Tsai A, Hsao Y-S, Li C-C, Cheng M Y

机构信息

Institute of Genetics, School of Life Sciences, National Yang-Ming University, 155 Li-nung St. Sec2, 112, Taipei, Taiwan, Republic of China.

出版信息

Mol Genet Genomics. 2003 Jun;269(3):321-30. doi: 10.1007/s00438-003-0835-1. Epub 2003 Mar 29.

Abstract

The yeast pet18 mutant exhibits three distinct phenotypes: temperature-sensitive lethality, failure to maintain a dsRNA virus, and respiration deficiency. We have isolated a yeast mutant, H53, with phenotypes identical to those of pet18. Based on PCR and Southern hybridization analysis, H53 was found to result from a large chromosomal deletion extending from YCR019w to YCR028c on chromosome III. Genetic analysis was carried out on H53 to correlate individual loci with each of the observed phenotypes. Disruption of YCR020c-a/MAK31 brought about a loss of dsRNA without affecting the temperature sensitive phenotype. The loss of YCR020w-b/HTL1, which encodes a hypothetical protein of 78 amino acids in length, was shown to be responsible for the temperature-sensitive lethality of the H53 mutant. Using immunoblotting, we demonstrated that a 7-kDa protein was indeed expressed in wild-type yeast, but not in a HTL1 deletion mutant. Moreover, the significance of HTL1 was investigated by isolating genes that are functionally associated with HTL1. We demonstrated that Rsc8p interacts physically with Htl1p, and that the genes RSC3, STH1 and RSC30 interact with HTL1. Thus, HTL1 may play a role in the function of the RSC complex.

摘要

酵母pet18突变体表现出三种不同的表型:温度敏感致死性、无法维持双链RNA病毒以及呼吸缺陷。我们分离出了一种酵母突变体H53,其表型与pet18相同。基于PCR和Southern杂交分析,发现H53是由III号染色体上从YCR019w延伸至YCR028c的大片段染色体缺失导致的。对H53进行了遗传分析,以将各个基因座与每种观察到的表型相关联。破坏YCR020c-a/MAK31导致双链RNA丢失,而不影响温度敏感表型。编码长度为78个氨基酸的假定蛋白的YCR020w-b/HTL1的缺失被证明是H53突变体温度敏感致死性的原因。通过免疫印迹,我们证明一种7 kDa的蛋白确实在野生型酵母中表达,但在HTL1缺失突变体中不表达。此外,通过分离与HTL1功能相关的基因来研究HTL1的重要性。我们证明Rsc8p与Htl1p发生物理相互作用,并且基因RSC3、STH1和RSC30与HTL1相互作用。因此,HTL1可能在RSC复合体的功能中发挥作用。

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