Disruption of the FG nucleoporin Nup98 causes selective changes in nuclear pore complex stoichiometry and function

Xiaosheng Wu, Lawryn H. Kasper, Ralitsa T. Mantcheva, George T. Mantchev, Margaret J. Springett, Jan Van Deursen

Research output: Contribution to journalArticle

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Abstract

The NUP98 gene encodes precursor proteins that generate two nucleoplasmically oriented nucleoporins, NUP98 and NUP96. By using gene targeting, we have selectively disrupted the murine NUP98 protein, leaving intact the expression and localization of NUP96. We show that NUP98 is essential for mouse gastrulation, a developmental stage that is associated with rapid cell proliferation, but dispensable for basal cell growth. NUP98-/- cells had an intact nuclear envelope with a normal number of embedded nuclear pore complexes. Typically, NUP98-deficient cells contained on average approximately 5-fold more cytoplasmic annulate lamellae than control cells. We found that a set of cytoplasmically oriented nucleoporins, including NUP358, NUP214, NUP88, and p62, assembled inefficiently into nuclear pores of NUP98-/- cells. Instead, these nucleoporins were prominently associated with the annulate lamellae. By contrast, a group of nucleoplasmically oriented nucleoporins, including NUP153, NUP50, NUP96, and NUP93, had no affinity for annulate lamellae and assembled normally into nuclear pores. Mutant pores were significantly impaired in transport receptor-mediated docking of proteins with a nuclear localization signal or M9 import signal and showed weak nuclear import of such substrates. In contrast, the ability of mutant pores to import ribosomal protein L23a and spliceosome protein U1A appeared intact. These observations show that NUP98 disruption selectively impairs discrete protein import pathways and support the idea that transport of distinct import complexes through the nuclear pore complex is mediated by specific subsets of nucleoporins.

Original languageEnglish (US)
Pages (from-to)3191-3196
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume98
Issue number6
DOIs
StatePublished - Mar 13 2001

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Nuclear Pore
Nuclear Pore Complex Proteins
Spliceosomes
Nuclear Localization Signals
Gastrulation
Proteins
Protein Precursors
Cell Nucleus Active Transport
Gene Targeting
nuclear pore complex protein 98
Ribosomal Proteins
Nuclear Envelope
Cell Proliferation

ASJC Scopus subject areas

  • Genetics
  • General

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Disruption of the FG nucleoporin Nup98 causes selective changes in nuclear pore complex stoichiometry and function. / Wu, Xiaosheng; Kasper, Lawryn H.; Mantcheva, Ralitsa T.; Mantchev, George T.; Springett, Margaret J.; Van Deursen, Jan.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 98, No. 6, 13.03.2001, p. 3191-3196.

Research output: Contribution to journalArticle

Wu, Xiaosheng ; Kasper, Lawryn H. ; Mantcheva, Ralitsa T. ; Mantchev, George T. ; Springett, Margaret J. ; Van Deursen, Jan. / Disruption of the FG nucleoporin Nup98 causes selective changes in nuclear pore complex stoichiometry and function. In: Proceedings of the National Academy of Sciences of the United States of America. 2001 ; Vol. 98, No. 6. pp. 3191-3196.
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