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首页> 外文期刊>Journal of Cell Science >Mcp6, a meiosis-specific coiled-coil protein of Schizosaccharomyces pombe, localizes to the spindle pole body and is required for horsetail movement and recombination
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Mcp6, a meiosis-specific coiled-coil protein of Schizosaccharomyces pombe, localizes to the spindle pole body and is required for horsetail movement and recombination

机译:Mcp6是粟酒裂殖酵母减数分裂特有的卷曲螺旋蛋白,位于纺锤极体,是马尾运动和重组所必需的

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摘要

We report here that a meiosis-specific gene of Schizosaccharomyces pombe denoted mcp(6+) (meiotic coiled-coil protein) encodes a protein that is required for the horsetail movement of chromosomes at meiosis I. The mcp(6+) gene is specifically transcribed during the horsetail phase. Green fluorescent protein (GFP)-tagged Mcp6 appears at the start of karyogamy, localizes to the spindle-pole body (SPB) and then disappears before chromosome segregation at meiosis I. In the mcp6Delta strain, the horsetail movement was either hampered (zygotic meiosis) or abolished (azygotic meiosis) and the pairing of homologous chromosomes was impaired. Accordingly, the allelic recombination rates of the mcp6Delta strain were only 10-40% of the wild-type rates. By contrast, the ectopic recombination rate of the mcp6Delta strainwas twice the wildtype rate. This is probably caused by abnormal homologous pairing in mcp6Delta cells because of aberrant horsetail movement. Fluorescent microscopy indicates that SPB components such as Sad1, Kms1 and Spo15 localize normally in mcp6Delta cells. Because Taz1 and Swi6 also localized with Sad1 in mcp6Delta cells, Mcp6 is not required for telomere clustering. In a taz1Delta strain, which does not display telomere clustering, and the dhc1-d3 mutant, which lacks horsetail movement, Mcp6 localized with Sad1 normally. However, we observed abnormal astral microtubule organization in mcp6Delta cells. From these results, we conclude that Mcp6 is necessary for neither SPB organization nor telomere clustering, but is required for proper astral microtubule positioning to maintain horsetail movement.
机译:我们在这里报告说,裂殖酵母的减数分裂特异性基因表示为mcp(6 +)(减数分裂卷曲螺旋蛋白)编码减数分裂I染色体的马尾运动所需的蛋白质。mcp(6+)基因是特定的在马尾阶段转录。带有绿色荧光蛋白(GFP)标签的Mcp6出现在核配子体的开始,定位于纺锤体(SPB),然后在减数分裂I染色体分离之前消失。在mcp6Delta菌株中,马尾运动受阻(合子减数分裂) )或被废除(合子减数分裂),同源染色体的配对受损。因此,mcp6Delta菌株的等位基因重组率仅为野生型率的10-40%。相反,mcp6Delta菌株的异位重组率是野生型率的两倍。这可能是由于异常的马尾运动导致mcp6Delta细胞中的异常同源配对引起的。荧光显微镜检查表明,SPB组件(例如Sad1,Kms1和Spo15)正常定位在mcp6Delta细胞中。因为Taz1和Swi6也在Sadp1中定位在mcp6Delta细胞中,所以端粒簇不需要Mcp6。在不显示端粒簇的taz1Delta菌株和缺少马尾运动的dhc1-d3突变体中,Mcp6通常定位在Sad1上。但是,我们在mcp6Delta细胞中观察到星状微管组织异常。从这些结果,我们得出结论,Mcp6既不是SPB组织也不是端粒簇所必需的,但对于正确的星形微管定位以维持马尾运动是必需的。

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