TY - JOUR
T1 - Acetylation in hormone signaling and the cell cycle
AU - Fu, Maofu
AU - Wang, Chenguang
AU - Wang, Jian
AU - Zafonte, Brian T.
AU - Lisanti, Michael P.
AU - Pestell, Richard G.
N1 - Funding Information:
We apologize to many authors for not citing their contributions due to space limitations. This work was supported by grants from NIH (R01CA70896, RO1CA75503, RO1CA86072, RO1 CA77552, RO1 DK53446), the Pfeiffer Foundation, The Susan Komen Breast Cancer Foundation, and Breast Cancer Alliance Inc. (to R.G.P.). M.P.L. was supported by grants from the National Institutes of Health (NIH), the Muscular Dystrophy Association (MDA), and the American Heart Association, as well as a Hirsch/Weil-Caulier Career Scientist Award.
PY - 2002
Y1 - 2002
N2 - The last decade has seen a substantial change in thinking about the role of acetylation in regulating diverse cellular processes. The correlation between histone acetylation and gene transcription has been known for many years. The cloning and biochemical characterization of the enzymes that regulate this post-translational modification has led to an understanding of the diverse role histone acetyltransferases (HATs) play in cellular function. Histone acetylases modify histones, transcription factors, co-activators, nuclear transport proteins, structural proteins and components of the cell cycle. This review focuses on the role of histone acetylases in coordinating hormone signaling and the cell cycle. Transition through the cell cycle is regulated by a family of protein kinase holoenzymes, the cyclin-dependent kinases (Cdks) and their heterodimeric cyclin partners. Recent studies have identified important cross-talk between the cell cycle regulatory apparatus and proteins regulating histone acetylation. The evidence for a dynamic interplay between components regulating the cell cycle and acetylation of target substrates provides an important new level of complexity in the mechanisms governing hormone signaling.
AB - The last decade has seen a substantial change in thinking about the role of acetylation in regulating diverse cellular processes. The correlation between histone acetylation and gene transcription has been known for many years. The cloning and biochemical characterization of the enzymes that regulate this post-translational modification has led to an understanding of the diverse role histone acetyltransferases (HATs) play in cellular function. Histone acetylases modify histones, transcription factors, co-activators, nuclear transport proteins, structural proteins and components of the cell cycle. This review focuses on the role of histone acetylases in coordinating hormone signaling and the cell cycle. Transition through the cell cycle is regulated by a family of protein kinase holoenzymes, the cyclin-dependent kinases (Cdks) and their heterodimeric cyclin partners. Recent studies have identified important cross-talk between the cell cycle regulatory apparatus and proteins regulating histone acetylation. The evidence for a dynamic interplay between components regulating the cell cycle and acetylation of target substrates provides an important new level of complexity in the mechanisms governing hormone signaling.
KW - Cyclin-dependent kinases
KW - Histone acetyltransferases
UR - http://www.scopus.com/inward/record.url?scp=0035992509&partnerID=8YFLogxK
U2 - 10.1016/S1359-6101(02)00003-5
DO - 10.1016/S1359-6101(02)00003-5
M3 - Review article
C2 - 12486878
AN - SCOPUS:0035992509
SN - 1359-6101
VL - 13
SP - 259
EP - 276
JO - Cytokine and Growth Factor Reviews
JF - Cytokine and Growth Factor Reviews
IS - 3
ER -