RETRACTED: Nuclear Receptor Function Requires a TFTC-Type Histone Acetyl Transferase Complex (Q55920649)

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Hirochika Kitagawa

2

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Mitsuaki Yanagida

3

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Osamu Wada

4

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Satoko Ogawa

5

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Madoka Nakagomi

6

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Hajime Oishi

7

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Yasuji Yamamoto

8

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Hiromich Nagasawa

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Steven B McMahon

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Michael D Cole

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Nobuhiro Takahashi

13

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Shigeaki Kato

AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer

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publication date

March 2002

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published in

Molecular Cell

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volume

9

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issue

3

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page(s)

553-562

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Identification of TATA-binding protein-free TAFII-containing complex subunits suggests a role in nucleosome acetylation and signal transduction

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Recruitment of HAT complexes by direct activator interactions with the ATM-related Tra1 subunit

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BRG-1 is recruited to estrogen-responsive promoters and cooperates with factors involved in histone acetylation

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Increasing the complexity of coactivation in nuclear receptor signaling

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A novel human SRB/MED-containing cofactor complex, SMCC, involved in transcription regulation

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A signature motif in transcriptional co-activators mediates binding to nuclear receptors

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Identity between TRAP and SMCC complexes indicates novel pathways for the function of nuclear receptors and diverse mammalian activators

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A novel protein complex that interacts with the vitamin D3 receptor in a ligand-dependent manner and enhances VDR transactivation in a cell-free system

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The transcriptional co-activator p/CIP binds CBP and mediates nuclear-receptor function

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The 400 kDa subunit of the PCAF histone acetylase complex belongs to the ATM superfamily

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