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Conserved and specific functions of mammalian ssu72

We describe the cloning and characterization of a human homolog of the yeast transcription/RNA-processing factor Ssu72, following a yeast two-hybrid screen for pRb-binding factors in the prostate gland. Interaction between hSsu72 and pRb was observed in transfected mammalian cells and involved multi...

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Autores principales: St-Pierre, Benoit, Liu, Xudong, Kha, Lan-Chau T., Zhu, Xudong, Ryan, Owen, Jiang, Zhe, Zacksenhaus, Eldad
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548335/
https://www.ncbi.nlm.nih.gov/pubmed/15659578
http://dx.doi.org/10.1093/nar/gki171
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author St-Pierre, Benoit
Liu, Xudong
Kha, Lan-Chau T.
Zhu, Xudong
Ryan, Owen
Jiang, Zhe
Zacksenhaus, Eldad
author_facet St-Pierre, Benoit
Liu, Xudong
Kha, Lan-Chau T.
Zhu, Xudong
Ryan, Owen
Jiang, Zhe
Zacksenhaus, Eldad
author_sort St-Pierre, Benoit
collection PubMed
description We describe the cloning and characterization of a human homolog of the yeast transcription/RNA-processing factor Ssu72, following a yeast two-hybrid screen for pRb-binding factors in the prostate gland. Interaction between hSsu72 and pRb was observed in transfected mammalian cells and involved multiple domains in pRb; however, so far, mutual effects of these two factors could not be demonstrated. Like the yeast counterpart, mammalian Ssu72 associates with TFIIB and the yeast cleavage/polyadenylation factor Pta1, and exhibits intrinsic phosphatase activity. Mammals contain a single ssu72 gene and a few pseudogenes. During mouse embryogenesis, ssu72 was highly expressed in the nervous system and intestine; high expression in the nervous system persisted in adult mice and was also readily observed in multiple human tumor cell lines. Both endogenous and ectopically expressed mammalian Ssu72 proteins resided primarily in the cytoplasm and only partly in the nucleus. Interestingly, fusion to a strong nuclear localization signal conferred nuclear localization only in a fraction of transfected cells, suggesting active tethering in the cytoplasm. Suppression of ssu72 expression in mammalian cells by siRNA did not reduce proliferation/survival, and its over-expression did not affect transcription of candidate genes in transient reporter assays. Despite high conservation, hssu72 was unable to rescue an ssu72 lethal mutation in yeast. Together, our results highlight conserved and mammalian specific characteristics of mammalian ssu72.
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spelling pubmed-5483352005-02-10 Conserved and specific functions of mammalian ssu72 St-Pierre, Benoit Liu, Xudong Kha, Lan-Chau T. Zhu, Xudong Ryan, Owen Jiang, Zhe Zacksenhaus, Eldad Nucleic Acids Res Article We describe the cloning and characterization of a human homolog of the yeast transcription/RNA-processing factor Ssu72, following a yeast two-hybrid screen for pRb-binding factors in the prostate gland. Interaction between hSsu72 and pRb was observed in transfected mammalian cells and involved multiple domains in pRb; however, so far, mutual effects of these two factors could not be demonstrated. Like the yeast counterpart, mammalian Ssu72 associates with TFIIB and the yeast cleavage/polyadenylation factor Pta1, and exhibits intrinsic phosphatase activity. Mammals contain a single ssu72 gene and a few pseudogenes. During mouse embryogenesis, ssu72 was highly expressed in the nervous system and intestine; high expression in the nervous system persisted in adult mice and was also readily observed in multiple human tumor cell lines. Both endogenous and ectopically expressed mammalian Ssu72 proteins resided primarily in the cytoplasm and only partly in the nucleus. Interestingly, fusion to a strong nuclear localization signal conferred nuclear localization only in a fraction of transfected cells, suggesting active tethering in the cytoplasm. Suppression of ssu72 expression in mammalian cells by siRNA did not reduce proliferation/survival, and its over-expression did not affect transcription of candidate genes in transient reporter assays. Despite high conservation, hssu72 was unable to rescue an ssu72 lethal mutation in yeast. Together, our results highlight conserved and mammalian specific characteristics of mammalian ssu72. Oxford University Press 2005 2005-01-19 /pmc/articles/PMC548335/ /pubmed/15659578 http://dx.doi.org/10.1093/nar/gki171 Text en © 2005, the authors Nucleic Acids Research, Vol. 33 No. 2 © Oxford University Press 2005; all rights reserved
spellingShingle Article
St-Pierre, Benoit
Liu, Xudong
Kha, Lan-Chau T.
Zhu, Xudong
Ryan, Owen
Jiang, Zhe
Zacksenhaus, Eldad
Conserved and specific functions of mammalian ssu72
title Conserved and specific functions of mammalian ssu72
title_full Conserved and specific functions of mammalian ssu72
title_fullStr Conserved and specific functions of mammalian ssu72
title_full_unstemmed Conserved and specific functions of mammalian ssu72
title_short Conserved and specific functions of mammalian ssu72
title_sort conserved and specific functions of mammalian ssu72
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548335/
https://www.ncbi.nlm.nih.gov/pubmed/15659578
http://dx.doi.org/10.1093/nar/gki171
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