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SPEF2基因可变剪切体和功能性SNP鉴定及其与公牛精液性状的相关性研究 被引量:3
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作者 郭芳 罗国静 +3 位作者 鞠志花 王秀革 黄金明 徐银学 《南京农业大学学报》 CAS CSCD 北大核心 2014年第3期119-125,共7页
为研究牛精子鞭毛2(SPEF2)基因在中国荷斯坦公牛各组织中的表达调控机制及其与精液品质的相关性,利用RTPCR和克隆测序技术分析SPEF2基因的可变剪切体,同时利用PCR-RFLP(PCR-restriction fragment length polymorphism)技术对中国荷斯坦... 为研究牛精子鞭毛2(SPEF2)基因在中国荷斯坦公牛各组织中的表达调控机制及其与精液品质的相关性,利用RTPCR和克隆测序技术分析SPEF2基因的可变剪切体,同时利用PCR-RFLP(PCR-restriction fragment length polymorphism)技术对中国荷斯坦公牛群体进行基因型检测分析。结果表明:鉴定到1个新转录本,命名为SPEF2-splice variant(SPEF2-SV),此转录本是从外显子2到外显子5之间缺失459 bp的新序列,预测编码1个含有1 618个氨基酸的蛋白。SPEF2基因的参考转录本在睾丸中高表达,而SPEF2-SV呈现低表达。在SPEF2基因第1内含子(邻近剪切位点附近140 bp)筛选到1个单核苷酸多态(SNP)突变位点(g.11043C>T),经ESEfinder 3.0软件预测发现该SNP改变了剪切因子结合蛋白SC35与靶序列的结合,它可能是产生异常转录本的重要原因。此SNP位点与中国荷斯坦公牛精液品质的相关性分析结果表明,其与射精量、精子密度和精子活力无显著相关,而与精子畸形率显著相关(P<0.05),其中等位基因对精子畸形的加性效应、显性和替代效应分别是-1.24%、-2.99%、-0.76%。结论:SPEF2基因表达受可变剪切机制的调控,而且其g.11043C>T突变位点可作为中国荷斯坦公牛精液品质选择的潜在功能性分子标记。 展开更多
关键词 精子鞭毛2基因 剪切增强子 单核苷酸多态性 公牛 精液品质
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Sperm flagellar 2(SPEF2)is essential for sperm flagellar assembly in humans 被引量:3
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作者 Dong-Yan Li Xiao-Xuan Yang +6 位作者 Chao-Feng Tu Wei-Li Wang Lan-Lan Meng Guang-Xiu Lu Yue-Qiu Tan Qian-Jun Zhang Juan Du 《Asian Journal of Andrology》 SCIE CAS CSCD 2022年第4期359-366,共8页
Spermiogenesis is a complex and tightly regulated process,consisting of acrosomal biogenesis,condensation of chromatin,flagellar assembly,and disposal of extra cytoplasm.Previous studies have reported that sperm flage... Spermiogenesis is a complex and tightly regulated process,consisting of acrosomal biogenesis,condensation of chromatin,flagellar assembly,and disposal of extra cytoplasm.Previous studies have reported that sperm flagellar 2(SPEF2)deficiency causes severe asthenoteratozoospermia owing to spermiogenesis failure,but the underlying molecular mechanism in humans remains unclear.Here,we performed proteomic analysis on spermatozoa from three SPEF2 mutant patients to study the functional role of SPEF2 during sperm tail development.A total of 1262 differentially expressed proteins were detected,including 486 upregulated and 776 downregulated.The constructed heat map of the differentially expressed proteins showed similar trends.Among these,the expression of proteins related to flagellar assembly,including SPEF2,sperm associated antigen 6(SPAG6),dynein light chain tctex-type 1(DYNLT1),radial spoke head component 1(RSPH1),translocase of outer mitochondrial membrane 20(TOM20),EF-hand domain containing 1(EFHC1),meiosis-specific nuclear structural 1(MNS1)and intraflagellar transport 20(IFT20),was verified by western blot.Functional clustering analysis indicated that these differentially expressed proteins were specifically enriched for terms such as spermatid development and flagellar assembly.Furthermore,we showed that SPEF2 interacts with radial spoke head component 9(RSPH9)and IFT20 in vitro,which are well-studied components of radial spokes or intra-flagellar transport and are essential for flagellar assembly.These results provide a rich resource for further investigation into the molecular mechanism underlying the role that SPEF2 plays in sperm tail development and could provide a theoretical basis for gene therapy in SPEF2 mutant patients in the future. 展开更多
关键词 spef2 flagellar assembly male infertility protein interaction PROTEOMICS
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