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Mitosin/CENP-F is a conserved kinetochore protein subjected to cyto plasmic dynein-mediated poleward transport 被引量:11
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作者 ZHEN YE YANG, JING GUO, NING LI, MIN QIAN, SHENG NIAN WANG, XUE LIANG ZHULaboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, China 《Cell Research》 SCIE CAS CSCD 2003年第4期275-283,共9页
Mitosin/CENP-F is a human nuclear protein transiently associated with the outer kinetochore plate in M phase and is involved in M phase progression. LEK1 and CMF1, which are its murine and chicken orthologs, however, ... Mitosin/CENP-F is a human nuclear protein transiently associated with the outer kinetochore plate in M phase and is involved in M phase progression. LEK1 and CMF1, which are its murine and chicken orthologs, however, are implicated in muscle differentiation and reportedly not distributed at kinetochores.We therefore conducted several assays to clarify this issue. The typical centromere staining patterns were observed in mitotic cells from both human primary culture and murine, canine, and mink cell lines. A C-terminal portion of LEK1 also conferred centromere localization. Our analysis further suggests conserved kinetochore localization of mammalian mitosin orthologs. Moreover, mitosin was associated preferentially with kinetochores of unaligned chromosomes. It was also constantly transported from kinetochores to spindle poles by cytoplasmic dynein. These properties resemble those of other kinetochore proteins important for the spindle checkpoint, thus implying a role of mitosin in this checkpoint. Therefore, mitosin family may serve as multifunctional proteins involved in both mitosis and differentiation. 展开更多
关键词 mitosin LEKl CENP-F kinetochore.
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中药金叶败毒颗粒抑制人巨细胞病毒感染丝裂素活化蛋白激酶p38信号通路的研究 被引量:4
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作者 汪辉 闻良珍 凌霞珍 《中国中西医结合杂志》 CAS CSCD 北大核心 2002年第11期838-840,共3页
目的 :研究金叶败毒颗粒 (简称中药 )对人巨细胞病毒 (HCMV)感染丝裂素活化蛋白激酶(MAPK) p38信号通路的抑制作用 ,并探讨其治疗HCMV感染的分子机制。 方法 :应用原位杂交和免疫组化方法分别检测中药和更昔洛韦 (GCV)干预HCMV感染的细... 目的 :研究金叶败毒颗粒 (简称中药 )对人巨细胞病毒 (HCMV)感染丝裂素活化蛋白激酶(MAPK) p38信号通路的抑制作用 ,并探讨其治疗HCMV感染的分子机制。 方法 :应用原位杂交和免疫组化方法分别检测中药和更昔洛韦 (GCV)干预HCMV感染的细胞 p38mRNA及 pRb蛋白表达水平 ,观察两种药物对HCMV感染人胚胎成纤维细胞 (HEL)的影响。结果 :两种药物均可抑制HCMV在HEL中的增殖 ,但中药能明显抑制 p38mRNA的水平 ,并使其磷酸化底物 pRb蛋白表达降低 ,而GCV无此作用。 结论 展开更多
关键词 中药 金叶败毒颗粒 人巨细胞病毒感染 丝裂素活化蛋白激酶 P38信号通路
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