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Primary sequence and heterologous expression of nuclear pore glycoprotein p62

The major nuclear pore protein p62 is modified by O-linked N- acetylglucosamine and functions in nuclear transport. We have cloned, sequenced, and expressed the full-length rat p62 cDNA. The rat p62 mRNA is 2,941 nucleotides long and encodes a protein of 525 amino acids containing 30% serine and thr...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1990
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2116139/
https://www.ncbi.nlm.nih.gov/pubmed/2190987
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description The major nuclear pore protein p62 is modified by O-linked N- acetylglucosamine and functions in nuclear transport. We have cloned, sequenced, and expressed the full-length rat p62 cDNA. The rat p62 mRNA is 2,941 nucleotides long and encodes a protein of 525 amino acids containing 30% serine and threonine residues. The amino acid sequence near the amino-terminus contains unique tetrapeptide repeats while the carboxy-terminus consists of a series of predicted alpha-helical regions with hydrophobic heptad repeats. Heterologous expression of rat p62 in African Green Monkey Kidney COS-1 cells and CV-1 cells was detected using a species-specific antipeptide serum. When transiently expressed in COS-1 cells, rat p62 binds wheat germ agglutinin and concentrates at the spindle poles during mitosis. In CV-1 cells cotransfected with rat p62 cDNA and SV40 viral DNA, rat p62 associates with the nuclear membrane without interfering with the nuclear transport of SV40 large T antigen. The ability to express p62 in tissue culture cells will facilitate analysis of the role of this pore protein in nuclear transport.
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spelling pubmed-21161392008-05-01 Primary sequence and heterologous expression of nuclear pore glycoprotein p62 J Cell Biol Articles The major nuclear pore protein p62 is modified by O-linked N- acetylglucosamine and functions in nuclear transport. We have cloned, sequenced, and expressed the full-length rat p62 cDNA. The rat p62 mRNA is 2,941 nucleotides long and encodes a protein of 525 amino acids containing 30% serine and threonine residues. The amino acid sequence near the amino-terminus contains unique tetrapeptide repeats while the carboxy-terminus consists of a series of predicted alpha-helical regions with hydrophobic heptad repeats. Heterologous expression of rat p62 in African Green Monkey Kidney COS-1 cells and CV-1 cells was detected using a species-specific antipeptide serum. When transiently expressed in COS-1 cells, rat p62 binds wheat germ agglutinin and concentrates at the spindle poles during mitosis. In CV-1 cells cotransfected with rat p62 cDNA and SV40 viral DNA, rat p62 associates with the nuclear membrane without interfering with the nuclear transport of SV40 large T antigen. The ability to express p62 in tissue culture cells will facilitate analysis of the role of this pore protein in nuclear transport. The Rockefeller University Press 1990-06-01 /pmc/articles/PMC2116139/ /pubmed/2190987 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Primary sequence and heterologous expression of nuclear pore glycoprotein p62
title Primary sequence and heterologous expression of nuclear pore glycoprotein p62
title_full Primary sequence and heterologous expression of nuclear pore glycoprotein p62
title_fullStr Primary sequence and heterologous expression of nuclear pore glycoprotein p62
title_full_unstemmed Primary sequence and heterologous expression of nuclear pore glycoprotein p62
title_short Primary sequence and heterologous expression of nuclear pore glycoprotein p62
title_sort primary sequence and heterologous expression of nuclear pore glycoprotein p62
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2116139/
https://www.ncbi.nlm.nih.gov/pubmed/2190987