Výsledky vyhledávání - "Moses O. Gold"

Targeting of CDK8 to a promoter-proximal RNA element demonstrates catalysis-dependent activation of gene expression

Publikováno v: Nucleic Acids Research. 26:3784-3788

During transcription of mRNA genes, there is a correlation between the phosphorylation state of the C-terminal domain (CTD) of the large subunit of RNA polymerase II (RNAP II) and the ability of the RNAP II complex to processively transcribe the gene

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a57665e55c2aab7e3d9dd125ed8ba7c
https://doi.org/10.1093/nar/26.16.3784

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PITALRE, the Catalytic Subunit of TAK, Is Required for Human Immunodeficiency Virus Tat Transactivation In Vivo

Autor: Andrew P. Rice, Christine H. Herrmann, Moses O. Gold, Xinzhen Yang

Publikováno v: Journal of Virology. 72:4448-4453

The human cdc2-related kinase PITALRE is the catalytic component of TAK, the Tat-associated kinase. Previously, we have proposed that TAK is a cellular factor that mediates Tat transactivation function. Here we demonstrate that transient overexpressi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::155eb1b5eafb57b643dcd4f4bf51b61b
https://doi.org/10.1128/jvi.72.5.4448-4453.1998

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Mutant adenovirus type 9 E4 ORF1 genes define three protein regions required for transformation of CREF cells

Autor: Moses O. Gold, Hannes Vogel, Ronald T. Javier, Robert S. Weiss

Publikováno v: Journal of Virology. 71:4385-4394

Human adenovirus type 9 (Ad9) elicits exclusively estrogen-dependent mammary tumors in rats, and an essential oncogenic determinant for this virus is Ad9 E4 open reading frame 1 (9ORF1), which encodes a 125-residue cytoplasmic protein with cellular g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccff5e5d5304de746f10f056d67238be
https://doi.org/10.1128/jvi.71.6.4385-4394.1997

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TAK, an HIV Tat-associated kinase, is a member of the cyclin-dependent family of protein kinases and is induced by activation of peripheral blood lymphocytes and differentiation of promonocytic cell lines

Autor: Estuardo Aguilar-Cordova, Christine H. Herrmann, Andrew P. Rice, Moses O. Gold, Xinzhen Yang, Dorothy E. Lewis, Derek N.G. Tang

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America. 94(23)

We have previously identified a cellular protein kinase activity termed TAK that specifically associates with the HIV types 1 and 2 Tat proteins. TAK hyperphosphorylates the carboxyl-terminal domain of the large subunit of RNA polymerase IIin vitroin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a7cee473c3455c8f2ffdc0a796f18df
https://pubmed.ncbi.nlm.nih.gov/9356449

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Viral transactivators E1A and VP16 interact with a large complex that is associated with CTD kinase activity and contains CDK8

Autor: Jean-Pierre Tassan, Erich A. Nigg, Moses O. Gold, Andrew P. Rice, Christine H. Herrmann

Publikováno v: Nucleic Acids Research, Vol. 24, No 19 (1996) pp. 3771-3777

Previously, we showed that the viral transactivator proteins E1A and VP16 specifically interact with a cellular CTD kinase activity in vitro. We now report that E1A and VP16 complexes contain human CDK8, a newly identified member of the cyclin-depend

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e187f2599a9ff9105e17b04478a62e8
https://pubmed.ncbi.nlm.nih.gov/8871557

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Viral transactivators specifically target distinct cellular protein kinases that phosphorylate the RNA polymerase II C-terminal domain

Autor: Moses O. Gold, Christine H. Herrmann, Andrew P. Rice

Publikováno v: Nucleic acids research. 24(3)

Phosphorylation of the carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II has been implicated as an important step in transcriptional regulation. Previously, we reported that a cellular CTD kinase, TAK, is targeted by the huma

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830145c434255fbaeadb6908e279614e
https://pubmed.ncbi.nlm.nih.gov/8602364

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