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Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression

Article Abstract:

Mad1 forms a complex with mSin3A and HDAC as evidenced by immunoprecipation by using [S]methionine-labeled 293epithelial cells. HDAC and Mad bind to separate regions of mSin3 as proved by using immunoprecipitation and transfection of 293 with plasmids expressing Mad1, HA-tagged Mad1, and HA-tagged Mad3. Mad1 repression requires histone deacetylase activity through formation of a ternary comlex with mSin3A and HDAC1/2 as proved by the effect of a specific histone deacetylase inhibitor on Mad1 transcriptional activity.

Author: Eisenman, Robert N., Laherty, Carol D., Seto, Edward, Yang, Wen-Ming, Davie, James R., Sun, Jian-Min
Publisher: Elsevier B.V.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 1997
Cytology, Animal genetics

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Linker histone H1 regulates specific gene expression but not global transcription in vivo

Article Abstract:

Previous research have failed to fully explain the role of linker histone in transcription in vivo. One way to remedy this problem is to look at Tetrahymena thermophila, a model system which provides a unique opportunity for elucidating on the linker histone function. Experiments show that the linker histone H1 knockout strain of Tetrahymena thermophila has no major effect on global transcription, although it acts as either a positive or negative gene-specific regulator of transcription in vivo.

Author: Shen, Xuetong, Gorovsky, Martin A.
Publisher: Elsevier B.V.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 1996

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A VSG expression site-associated gene confers resistance to human serum in Trypanosoma rhodesiense

Article Abstract:

A study was performed to demonstrate that the serum-resistance-associated (SRA) gene is an expression site-associated gene of the Edinburgh trypanozoon antigen type 1.10 (ETat 1.10) expression site. The SRA gene was encoded a variant surface glycoprotein-like protein and was only present in the R clones of the ETat strain of the Trypanosoma brucei rhodesiense resistant to normal human serum. Results revealed that SRA resulted to the resistance of the organism against normal human serum.

Author: Vanhamme, Luc, Pays, Annette, Pays, Etienne, Xong, Hoang Van, Chamekh, Mustapha, Chimfwembe, Chibeka Evelyn, Abbeele, Jan van den, Meirvenne, Nestor van, Hamers, Raymond, Baetselier, Patrick de
Publisher: Elsevier B.V.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 1998
Drug resistance in microorganisms, Microbial drug resistance, Serum, Blood serum, Trypanosoma brucei

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Subjects list: Research, Genetic aspects, Histones, Genetic transcription, Transcription (Genetics), Gene expression
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