Nogami Satoru, Fukuda Tomoyuki, Nagai Yuri, Yabe Shizu, Sugiura Masako, Mizutani Ryuta, Satow Yoshinori, Anraku Yasuhiro, Ohya Yoshikazu
Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, Bldg. FSB-101, 5-1-5 Kashiwanoha, Kashiwa, Chiba Prefecture, 277-8562 Japan.
Yeast. 2002 Jun 30;19(9):773-82. doi: 10.1002/yea.872.
PI-SceI (VDE), a homing endonuclease with protein splicing activity, is a genomic parasite in the VMA1 gene of Saccharomyces cerevisiae. In a heterozygous diploid of the VDE-less VMA1 allele and a VDE-containing VMA1 allele, VDE specifically cleaves its recognition sequence (VRS) in the VDE-less VMA1 allele at meiosis, followed by 'homing', i.e. a conversion to a VDE-containing allele. We found that upon VDE expression, homing of a marker gene at an extragenic locus occurs only when a 45 bp element containing the VRS is inserted at its allelic site, while mutants of VDE with no endonuclease activity lack authentic extragenic homing activity. Thus, both the VRS and VDE are required for homing. Insertion of the VRS in a homozygous diploid significantly lowered the spore germination ability, indicating that a template for gene repair at its allelic locus is essential for efficient homing and survival of yeast cells.
PI-SceI(VDE)是一种具有蛋白质剪接活性的归巢内切酶,是酿酒酵母VMA1基因中的一种基因组寄生虫。在不含VDE的VMA1等位基因和含VDE的VMA1等位基因的杂合二倍体中,VDE在减数分裂时特异性切割不含VDE的VMA1等位基因中的识别序列(VRS),随后进行“归巢”,即将其转化为含VDE的等位基因。我们发现,在VDE表达时,只有当一个包含VRS的45bp元件插入到其等位基因位点时,位于基因外位点的标记基因才会发生归巢,而没有内切酶活性的VDE突变体则缺乏真正的基因外归巢活性。因此,归巢需要VRS和VDE两者。在纯合二倍体中插入VRS会显著降低孢子萌发能力,这表明在其等位基因位点进行基因修复的模板对于酵母细胞的有效归巢和存活至关重要。