期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
Arabidopsis PTD Is Required for Type Ⅰ Crossover Formation and Affects Recombination Frequency in Two Different Chromosomal Regions 被引量:5
1
作者 Pingli Lu Asela J.Wijeratne +2 位作者 Zhengjia Wang Gregory P.Copenhaver Hong Ma 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2014年第3期165-175,共11页
In eukaryotes, crossovers together with sister chromatid cohesion maintain physical association between homologous chromosomes, ensuring accurate chromosome segregation during meiosis I and resulting in exchange of ge... In eukaryotes, crossovers together with sister chromatid cohesion maintain physical association between homologous chromosomes, ensuring accurate chromosome segregation during meiosis I and resulting in exchange of genetic information between homologues. The Arabidopsis PTD (Parting Dancers) gene affects the level of meiotic crossover formation, but its functional relationships with other core meiotic genes, such as AtSP011-1, AtRAD51, and AtMSH4, are unclear; whether PTD has other functions in meiosis is also unknown. To further analyze PTD function and to test for epistatic relationships, we compared the meiotic chromosome behaviors ofAtspoll-1 ptd and Atrad51 ptd double mutants with the relevant single mutants. The results suggest that PTD functions downstream of AtSP011-1 and AtRAD51 in the meiotic recombination pathway. Furthermore, we found that meiotic defects in rck pM and Atmsh4 ptd double mutants showed similar meiotic phenotypes to those of the relevant single mutants, providing genetic evidences for roles of PTD and RCK in the type I crossovers pathway. Moreover, we employed a pollen tetrad-based fluorescence method and found that the meiotic crossover frequencies in two genetic intervals were significantly reduced from 6.63% and 22.26% in wild-type to 1.14% and 6.36%, respectively, in the ptd^2 mutant. These results revealed new aspects of PTD function in meiotic crossover formation. 展开更多
关键词 PTD MEIOSIS msh4 CROSSOVER Recombination frequency
原文传递
山羊MSH4和MSH5基因的cDNA克隆、序列分析及组织表达
2
作者 郑杰 刘霜 +3 位作者 罗斌 胡亮 杨珂伟 字向东 《生物技术通报》 CAS CSCD 北大核心 2016年第3期98-104,共7页
以低繁藏山羊和高繁金堂黑山羊为研究对象,分别提取处于发情期的5只藏山羊和5只金堂黑山羊的卵巢、子宫、输卵管、垂体的总RNA,并通过RT-PCR技术对MSH4、MSH5基因c DNA进行克隆、序列分析,以Real-time PCR技术对其进行组织表达研究。结... 以低繁藏山羊和高繁金堂黑山羊为研究对象,分别提取处于发情期的5只藏山羊和5只金堂黑山羊的卵巢、子宫、输卵管、垂体的总RNA,并通过RT-PCR技术对MSH4、MSH5基因c DNA进行克隆、序列分析,以Real-time PCR技术对其进行组织表达研究。结果表明,藏山羊和金堂黑山羊MSH4基因编码区均长2 499 bp,编码832个氨基酸,两品种基因编码区有5处碱基不同,并导致3处氨基酸的差异;MSH5基因编码区均长2 496 bp,编码831个氨基酸,两品种基因编码区有9处碱基不同,并导致5处氨基酸的差异。藏山羊MSH4基因编码区核苷酸序列与金堂黑山羊、山羊、绵羊、牛、马、小鼠、褐家鼠、人的同源性分别为:99.8%、99.8%、99.4%、98.1%、94.4%、85.1%、84.7%和93.5%;藏山羊MSH5基因编码区核苷酸序列与金堂黑山羊、山羊、牛、家犬、小鼠、褐家鼠、人的同源性分别为:99.6%、99.6%、97.3%、88.0%、85.8%、85.3%和90.2%。MSH4和MSH5基因m RNA在两个山羊品种的卵巢、子宫、输卵管、垂体中均有表达,但两品种间无显著性差异(P>0.05)。说明MSH4和MSH5基因在动物进化中比较保守,与山羊多羔性状的相关性有待进一步研究。 展开更多
关键词 藏山羊 金堂黑山羊 msh4 msh5 克隆 定量PCR
下载PDF
牦牛和犏牛睾丸组织Msh4基因mRNA表达差异的研究 被引量:5
3
作者 曾琴 黄林 +2 位作者 金素钰 林亚秋 郑玉才 《黑龙江畜牧兽医》 CAS 北大核心 2013年第6期62-64,191,192,共5页
为了研究牦牛与犏牛睾丸组织Msh4基因mRNA表达水平的差异,从分子水平上揭示犏牛雄性不育的分子机制,试验从成年麦洼牦牛(n=9)、成年不育犏牛(n=3)和性未成熟犊牦牛(n=3)睾丸组织中提取总RNA,采用荧光定量PCR方法对Msh4 mRNA表达水平进... 为了研究牦牛与犏牛睾丸组织Msh4基因mRNA表达水平的差异,从分子水平上揭示犏牛雄性不育的分子机制,试验从成年麦洼牦牛(n=9)、成年不育犏牛(n=3)和性未成熟犊牦牛(n=3)睾丸组织中提取总RNA,采用荧光定量PCR方法对Msh4 mRNA表达水平进行检测。结果表明:犏牛和犊牦牛睾丸组织中Msh4 mRNA表达水平极显著低于牦牛(P<0.01),说明睾丸组织Msh4基因的低表达可能与犏牛雄性不育有关。 展开更多
关键词 牦牛 犏牛 杂交 雄性不育 睾丸 msh4基因
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部