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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...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2005
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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. |
format | Text |
id | pubmed-548335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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