TY - JOUR
T1 - Histone variants
T2 - Emerging players in cancer biology
AU - Vardabasso, Chiara
AU - Hasson, Dan
AU - Ratnakumar, Kajan
AU - Chung, Chi Yeh
AU - Duarte, Luis F.
AU - Bernstein, Emily
N1 - Funding Information:
The authors thank Zulekha Qadeer and Alexandre Gaspar-Maia for critically reading this manuscript. The authors thank Matthew O’Connell for microscopy assistance and Pablo DeIoannes for assistance with in silico homology modeling. This work is supported by an NCI T32-CA078207 to L.F.D, a Melanoma Research Development Award (Department of Dermatology, Mount Sinai) to C.V., and The Ellison Medical Foundation New Scholar Award, Association for International Cancer Research, Hirschl/Weill-Caulier Research Award and NCI/NIH R01CA154683 to E.B.
PY - 2014/2
Y1 - 2014/2
N2 - Histone variants are key players in shaping chromatin structure, and, thus, in regulating fundamental cellular processes such as chromosome segregation and gene expression. Emerging evidence points towards a role for histone variants in contributing to tumor progression, and, recently, the first cancer-associated mutation in a histone variant-encoding gene was reported. In addition, genetic alterations of the histone chaperones that specifically regulate chromatin incorporation of histone variants are rapidly being uncovered in numerous cancers. Collectively, these findings implicate histone variants as potential drivers of cancer initiation and/or progression, and, therefore, targeting histone deposition or the chromatin remodeling machinery may be of therapeutic value. Here, we review the mammalian histone variants of the H2A and H3 families in their respective cellular functions, and their involvement in tumor biology.
AB - Histone variants are key players in shaping chromatin structure, and, thus, in regulating fundamental cellular processes such as chromosome segregation and gene expression. Emerging evidence points towards a role for histone variants in contributing to tumor progression, and, recently, the first cancer-associated mutation in a histone variant-encoding gene was reported. In addition, genetic alterations of the histone chaperones that specifically regulate chromatin incorporation of histone variants are rapidly being uncovered in numerous cancers. Collectively, these findings implicate histone variants as potential drivers of cancer initiation and/or progression, and, therefore, targeting histone deposition or the chromatin remodeling machinery may be of therapeutic value. Here, we review the mammalian histone variants of the H2A and H3 families in their respective cellular functions, and their involvement in tumor biology.
KW - Cancer
KW - Chromatin remodeler
KW - Histone chaperones
KW - Histone post-translational modifications
KW - Histone variants
UR - http://www.scopus.com/inward/record.url?scp=84892755806&partnerID=8YFLogxK
U2 - 10.1007/s00018-013-1343-z
DO - 10.1007/s00018-013-1343-z
M3 - Review article
C2 - 23652611
AN - SCOPUS:84892755806
SN - 1420-682X
VL - 71
SP - 379
EP - 404
JO - Cellular and Molecular Life Sciences
JF - Cellular and Molecular Life Sciences
IS - 3
ER -