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通过ESCRT-III/Vps4对核孔复合体组装进行监测。

Surveillance of nuclear pore complex assembly by ESCRT-III/Vps4.

作者信息

Webster Brant M, Colombi Paolo, Jäger Jens, Lusk C Patrick

机构信息

Department of Cell Biology, Yale School of Medicine, New Haven, CT 06520, USA.

Department of Cell Biology, Yale School of Medicine, New Haven, CT 06520, USA.

出版信息

Cell. 2014 Oct 9;159(2):388-401. doi: 10.1016/j.cell.2014.09.012.

Abstract

The maintenance of nuclear compartmentalization by the nuclear envelope and nuclear pore complexes (NPCs) is essential for cell function; loss of compartmentalization is associated with cancers, laminopathies, and aging. We uncovered a pathway that surveils NPC assembly intermediates to promote the formation of functional NPCs. Surveillance is mediated by Heh2, a member of the LEM (Lap2-emerin-MAN1) family of integral inner nuclear membrane proteins, which binds to an early NPC assembly intermediate, but not to mature NPCs. Heh2 recruits the endosomal sorting complex required for transport (ESCRT)-III subunit Snf7 and the AAA-ATPase Vps4 to destabilize and clear defective NPC assembly intermediates. When surveillance or clearance is compromised, malformed NPCs accumulate in a storage of improperly assembled nuclear pore complexes compartment, or SINC. The SINC is retained in old mothers to prevent loss of daughter lifespan, highlighting a continuum of mechanisms to ensure nuclear compartmentalization.

摘要

核膜和核孔复合体(NPC)维持核区室化对于细胞功能至关重要;区室化的丧失与癌症、核纤层蛋白病和衰老相关。我们发现了一条监测NPC组装中间体以促进功能性NPC形成的途径。监测由Heh2介导,Heh2是内核膜整合蛋白LEM(Lap2-emerin-MAN1)家族的成员,它与早期NPC组装中间体结合,但不与成熟NPC结合。Heh2招募运输所需的内体分选复合体(ESCRT)-III亚基Snf7和AAA-ATP酶Vps4,以破坏并清除有缺陷的NPC组装中间体。当监测或清除功能受损时,畸形的NPC会积聚在错误组装的核孔复合体储存区,即SINC中。SINC保留在衰老的母细胞中以防止子细胞寿命缩短,这突出了确保核区室化的一系列机制。

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