Family with Sequence Similarity 60A (FAM60A) Protein Is a Cell Cycle-fluctuating Regulator of the SIN3-HDAC1 Histone Deacetylase Complex. / Munoz, Ivan M.; Macartney, Thomas; Sanchez-Pulido, Luis; Ponting, Chris P.; Rocha, Sonia; Rouse, John.
In: Journal of Biological Chemistry, Vol. 287, No. 39, 21.09.2012, p. 32346-53.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Family with Sequence Similarity 60A (FAM60A) Protein Is a Cell Cycle-fluctuating Regulator of the SIN3-HDAC1 Histone Deacetylase Complex
A1 - Munoz,Ivan M.
A1 - Macartney,Thomas
A1 - Sanchez-Pulido,Luis
A1 - Ponting,Chris P.
A1 - Rocha,Sonia
A1 - Rouse,John
AU - Munoz,Ivan M.
AU - Macartney,Thomas
AU - Sanchez-Pulido,Luis
AU - Ponting,Chris P.
AU - Rocha,Sonia
AU - Rouse,John
PY - 2012/9/21
Y1 - 2012/9/21
N2 - The SIN3A-HDAC complex deacetylates histones thereby repressing gene transcription. Here we describe family with sequence similarity 60A (FAM60A), a cell cycle-regulated protein that binds to the SIN3-HDAC complex. FAM60A expression peaks during G(1) and S phases of the cell cycle in U2OS cells, in a manner similar to the G(1) regulator cyclin D1, which is a known target of SIN3-HDAC. In this light we found that FAM60A binds to SIN3-HDAC-regulated promoters such as cyclin D1 in G(1) and S phases. Cells depleted of FAM60A show increased histone acetylation at the cyclin D1 promoter and elevated levels of cyclin D1 mRNA and protein. Furthermore, depletion of FAM60A altered the periodic association of HDAC1 with the cyclin D1 promoter, increased cyclin D1 expression at all cell cycle phases, and caused premature S phase entry. The data in this study introduce FAM60A as a novel regulator of SIN3-HDAC function and gene expression.
AB - The SIN3A-HDAC complex deacetylates histones thereby repressing gene transcription. Here we describe family with sequence similarity 60A (FAM60A), a cell cycle-regulated protein that binds to the SIN3-HDAC complex. FAM60A expression peaks during G(1) and S phases of the cell cycle in U2OS cells, in a manner similar to the G(1) regulator cyclin D1, which is a known target of SIN3-HDAC. In this light we found that FAM60A binds to SIN3-HDAC-regulated promoters such as cyclin D1 in G(1) and S phases. Cells depleted of FAM60A show increased histone acetylation at the cyclin D1 promoter and elevated levels of cyclin D1 mRNA and protein. Furthermore, depletion of FAM60A altered the periodic association of HDAC1 with the cyclin D1 promoter, increased cyclin D1 expression at all cell cycle phases, and caused premature S phase entry. The data in this study introduce FAM60A as a novel regulator of SIN3-HDAC function and gene expression.
U2 - 10.1074/jbc.M112.382499
DO - 10.1074/jbc.M112.382499
M1 - Article
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 39
VL - 287
SP - 32346
EP - 32353
ER -