Isolation and characterization of nuclear envelopes from the yeast Saccharomyces - PubMed (original) (raw)
Isolation and characterization of nuclear envelopes from the yeast Saccharomyces
C Strambio-de-Castillia et al. J Cell Biol. 1995 Oct.
Abstract
We have developed a large scale enrichment procedure to prepare yeast nuclear envelopes (NEs). These NEs can be stripped of peripheral proteins to produce a heparin-extracted NE (H-NE) fraction highly enriched in integral membrane proteins. Extraction of H-NEs with detergents revealed previously uncharacterized ring structures associated with the NE that apparently stabilize the grommets of the nuclear pore complexes (NPCs). The high yields obtained throughout the fractionation procedure allowed balance-sheet tabulation of the subcellular distribution of various NE and non-NE proteins. Thus we found that 20% of endoplasmic reticulum (ER) marker proteins are localized at the NE. Using a novel monospecific mAb made against proteins in the H-NE fraction and found to be directed against the pore membrane protein POM152, we showed that while the majority of POM152 is localized in the NE at the NPC, a proportion of this protein is also present in the ER. This ER pool of POM152 is likely to be involved in the duplication of nuclear pores and NPCs during S-phase. Both the NEs and H-NEs were found to be competent for the in vitro posttranslational translocation of prepro-alpha-factor. They may also be suitable to investigate other ER- and NE-associated functions in cell-free systems.
Similar articles
- Saccharomyces cerevisiae Ndc1p is a shared component of nuclear pore complexes and spindle pole bodies.
Chial HJ, Rout MP, Giddings TH, Winey M. Chial HJ, et al. J Cell Biol. 1998 Dec 28;143(7):1789-800. doi: 10.1083/jcb.143.7.1789. J Cell Biol. 1998. PMID: 9864355 Free PMC article. - Sec66-Dependent Regulation of Yeast Spindle-Pole Body Duplication Through Pom152.
Katta SS, Chen J, Gardner JM, Friederichs JM, Smith SE, Gogol M, Unruh JR, Slaughter BD, Jaspersen SL. Katta SS, et al. Genetics. 2015 Dec;201(4):1479-95. doi: 10.1534/genetics.115.178012. Epub 2015 Oct 28. Genetics. 2015. PMID: 26510791 Free PMC article. - Isolation of the yeast nuclear pore complex.
Rout MP, Blobel G. Rout MP, et al. J Cell Biol. 1993 Nov;123(4):771-83. doi: 10.1083/jcb.123.4.771. J Cell Biol. 1993. PMID: 8227139 Free PMC article. - Isolation and fractionation of rat liver nuclear envelopes and nuclear pore complexes.
Matunis MJ. Matunis MJ. Methods. 2006 Aug;39(4):277-83. doi: 10.1016/j.ymeth.2006.06.003. Methods. 2006. PMID: 16870471 Review. - Identification of novel integral membrane proteins of the nuclear envelope with potential disease links using subtractive proteomics.
Schirmer EC, Florens L, Guan T, Yates JR 3rd, Gerace L. Schirmer EC, et al. Novartis Found Symp. 2005;264:63-76; discussion 76-80, 227-30. Novartis Found Symp. 2005. PMID: 15773748 Review.
Cited by
- Distinct subcellular localization patterns contribute to functional specificity of the Cln2 and Cln3 cyclins of Saccharomyces cerevisiae.
Miller ME, Cross FR. Miller ME, et al. Mol Cell Biol. 2000 Jan;20(2):542-55. doi: 10.1128/MCB.20.2.542-555.2000. Mol Cell Biol. 2000. PMID: 10611233 Free PMC article. - Saccharomyces cerevisiae Ndc1p is a shared component of nuclear pore complexes and spindle pole bodies.
Chial HJ, Rout MP, Giddings TH, Winey M. Chial HJ, et al. J Cell Biol. 1998 Dec 28;143(7):1789-800. doi: 10.1083/jcb.143.7.1789. J Cell Biol. 1998. PMID: 9864355 Free PMC article. - The karyopherin Kap95 regulates nuclear pore complex assembly into intact nuclear envelopes in vivo.
Ryan KJ, Zhou Y, Wente SR. Ryan KJ, et al. Mol Biol Cell. 2007 Mar;18(3):886-98. doi: 10.1091/mbc.e06-06-0525. Epub 2006 Dec 20. Mol Biol Cell. 2007. PMID: 17182855 Free PMC article. - GFP-labelling of 26S proteasomes in living yeast: insight into proteasomal functions at the nuclear envelope/rough ER.
Enenkel C, Lehmann A, Kloetzel PM. Enenkel C, et al. Mol Biol Rep. 1999 Apr;26(1-2):131-5. doi: 10.1023/a:1006973803960. Mol Biol Rep. 1999. PMID: 10363659 Review. - Motor-driven motility of fungal nuclear pores organizes chromosomes and fosters nucleocytoplasmic transport.
Steinberg G, Schuster M, Theisen U, Kilaru S, Forge A, Martin-Urdiroz M. Steinberg G, et al. J Cell Biol. 2012 Aug 6;198(3):343-55. doi: 10.1083/jcb.201201087. Epub 2012 Jul 30. J Cell Biol. 2012. PMID: 22851316 Free PMC article.
References
- Cell. 1990 Jun 15;61(6):965-78 - PubMed
- J Cell Biol. 1990 Nov;111(5 Pt 1):1913-27 - PubMed
- J Biol Chem. 1988 May 5;263(13):6209-14 - PubMed
- Cell. 1993 Jun 18;73(6):1197-206 - PubMed
- Trends Cell Biol. 1994 Oct;4(10):357-65 - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases