NDC1: a crucial membrane-integral nucleoporin of metazoan nuclear pore complexes

Author:

Stavru Fabrizia12,Hülsmann Bastian B.12,Spang Anne3,Hartmann Enno4,Cordes Volker C.1,Görlich Dirk12

Affiliation:

1. Zentrum für Molekulare Biologie der Universität Heidelberg, D-69120 Heidelberg, Germany

2. Max-Planck-Institut für Biophysikalische Chemie, D-37077 Göttingen, Germany

3. Friedrich Miescher Laboratorium, Max-Planck-Gesellschaft, D-72076 Tübingen, Germany

4. Institut für Biologie, Universität Lübeck, D-23538 Lübeck, Germany

Abstract

POM121 and gp210 were, until this point, the only known membrane-integral nucleoporins (Nups) of vertebrates and, thus, the only candidate anchors for nuclear pore complexes (NPCs) within the nuclear membrane. In an accompanying study (see Stavru et al. on p. 477 of this issue), we provided evidence that NPCs can exist independently of POM121 and gp210, and we predicted that vertebrate NPCs contain additional membrane-integral constituents. We identify such an additional membrane protein in the NPCs of mammals, frogs, insects, and nematodes as the orthologue to yeast Ndc1p/Cut11p. Human NDC1 (hNDC1) likely possesses six transmembrane segments, and it is located at the nuclear pore wall. Depletion of hNDC1 from human HeLa cells interferes with the assembly of phenylalanine-glycine repeat Nups into NPCs. The loss of NDC1 function in Caenorhabditis elegans also causes severe NPC defects and very high larval and embryonic mortality. However, it is not ultimately lethal. Instead, homozygous NDC1-deficient worms can be propagated. This indicates that none of the membrane-integral Nups is universally essential for NPC assembly, and suggests that NPC biogenesis is an extremely fault-tolerant process.

Publisher

Rockefeller University Press

Subject

Cell Biology

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