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核纤层蛋白和emerin在间期细胞核中的共定位以及有丝分裂期间的变化。

Colocalization of emerin and lamins in interphase nuclei and changes during mitosis.

作者信息

Manilal S, Nguyen T M, Morris G E

机构信息

MRIC Biochemistry Group, N.E. Wales Institute, Wrexham, United Kingdom.

出版信息

Biochem Biophys Res Commun. 1998 Aug 28;249(3):643-7. doi: 10.1006/bbrc.1998.9209.

DOI:10.1006/bbrc.1998.9209
PMID:9731189
Abstract

Emerin is a nuclear membrane protein which is affected by mutation in X-linked Emery-Dreifuss muscular dystrophy. We have previously suggested that emerin is a member of a family of type II integral membrane proteins which associate with the nuclear lamina and which include lamina-associated proteins and the lamin B receptor. We now show that emerin in COS cells is not restricted to the nuclear rim but is also found at intranuclear sites, where it colocalizes with nuclear lamins B1, B2 and A/C. During mitosis, emerin is dispersed throughout the cell and then participates in the reconstitution of membranes around the daughter nuclei. Although emerin and lamins do not remain colocalized during mitosis, they all show some association with the midbody of the mitotic spindle.

摘要

Emerin是一种核膜蛋白,在X连锁的埃默里-德赖富斯肌营养不良症中会因突变而受到影响。我们之前曾提出,Emerin是II型整合膜蛋白家族的成员,该家族与核纤层相关,包括核纤层相关蛋白和核纤层B受体。我们现在发现,COS细胞中的Emerin不仅局限于核边缘,还存在于核内位点,在那里它与核纤层蛋白B1、B2和A/C共定位。在有丝分裂期间,Emerin分散在整个细胞中,然后参与子核周围膜的重建。虽然Emerin和核纤层蛋白在有丝分裂期间不会保持共定位,但它们都与有丝分裂纺锤体的中间体有一定关联。

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Colocalization of emerin and lamins in interphase nuclei and changes during mitosis.核纤层蛋白和emerin在间期细胞核中的共定位以及有丝分裂期间的变化。
Biochem Biophys Res Commun. 1998 Aug 28;249(3):643-7. doi: 10.1006/bbrc.1998.9209.
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The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.埃默菌素的细胞周期依赖性定位错误可能导致埃默里-德赖富斯肌营养不良症的表型。
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Both emerin and lamin C depend on lamin A for localization at the nuclear envelope.Emerin和核纤层蛋白C都依赖于核纤层蛋白A定位于核膜。
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Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy.不同类型埃默里-德赖富斯肌营养不良症患者肌肉中emerin和核纤层蛋白的表达
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How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?Emerin基因中的G993T突变是如何导致埃默里-德赖富斯肌营养不良症的?
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The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.埃默里-德赖富斯肌营养不良症的表型源于内核膜上emerin的异常靶向和结合。
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Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy.不同区域决定了emerin的核膜靶向定位,emerin是埃默里-德赖富斯肌营养不良症的致病蛋白。
Eur J Biochem. 1999 Feb;259(3):859-65. doi: 10.1046/j.1432-1327.1999.00112.x.
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Emerin Is Required for Proper Nucleus Reassembly after Mitosis: Implications for New Pathogenetic Mechanisms for Laminopathies Detected in EDMD1 Patients.emerin 在有丝分裂后细胞核正确重装配中是必需的:对 EDMD1 患者中检测到的核纤层蛋白病的新发病机制的影响。
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