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粗糙脉孢菌mei-3基因的鉴定与表达,该基因编码一种与酿酒酵母Rad51同源的蛋白质。

Identification and expression of the Neurospora crassa mei-3 gene which encodes a protein homologous to Rad51 of Saccharomyces cerevisiae.

作者信息

Hatakeyama S, Ishii C, Inoue H

机构信息

Department of Regulation Biology Faculty of Science, Saitama University, Urawa, Japan.

出版信息

Mol Gen Genet. 1995 Dec 10;249(4):439-46. doi: 10.1007/BF00287106.

Abstract

The mei-3 gene of Neurospora crassa encodes a homolog of the Escherichia coli RecA and Saccharomyces cerevisiae Rad51 proteins, which are required for recombination and repair of DNA double-strand breaks. To determine the molecular function of MEI3 protein, anti-MEI3 antibody was prepared and used in Western blot analysis. The antibody cross-reacted only with crude extracts prepared from perithecia, the fruiting bodies of Neurospora. The molecular weight of the MEI3 protein was estimated to be 38 kDa. Transformation experiments showed that a DNA fragment longer than previously reported was needed to complement the mei-3 mutation. On sequencing cDNA and genomic DNA, one open reading frame (ORF) was found, which consists of three exons interrupted by two small introns. This ORF encoded a MEI3 protein of 353 amino acids, and the inferred MW of 38 kDa is in good agreement with the results from Western blot analysis. Comparisons of MEI3 with other Rad51 homologs indicated that MEI3 protein contains the two conserved core domains (I and II) generally observed in Rad51 homologs in eukaryotes. Northern blot analysis showed that expression of mei-3 was raised remarkably after UV-irradiation or methyl methanesulfonate (MMS)-treatment. The transcript size was 1.6 kb and this was also larger than was reported previously.

摘要

粗糙脉孢菌的mei-3基因编码大肠杆菌RecA和酿酒酵母Rad51蛋白的同源物,这些蛋白是DNA双链断裂的重组和修复所必需的。为了确定MEI3蛋白的分子功能,制备了抗MEI3抗体并用于蛋白质免疫印迹分析。该抗体仅与从脉孢菌的子囊果(子实体)制备的粗提物发生交叉反应。MEI3蛋白的分子量估计为38 kDa。转化实验表明,需要一段比先前报道的更长的DNA片段来互补mei-3突变。对cDNA和基因组DNA进行测序时,发现了一个开放阅读框(ORF),它由三个外显子组成,中间被两个小内含子打断。这个ORF编码一个由353个氨基酸组成的MEI3蛋白,推断的分子量为38 kDa,与蛋白质免疫印迹分析的结果高度一致。将MEI3与其他Rad51同源物进行比较表明,MEI3蛋白含有真核生物Rad51同源物中普遍存在的两个保守核心结构域(I和II)。Northern印迹分析表明,在紫外线照射或甲基磺酸甲酯(MMS)处理后,mei-3的表达显著升高。转录本大小为1.6 kb,这也比先前报道的要大。

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