The novel BORIS+CTCF gene family is uniquely involved in the epigenetics of normal biology and cancer

被引:220
作者
Klenova, EA
Morse, HC
Ohlsson, RF
Lobanenkov, VV
机构
[1] NIAID, Immunopathol Lab, Sect Mol Pathol, NIH, Rockville, MD 20852 USA
[2] Univ Essex, Dept Biol Sci, Colchester CQ4 3SQ, Essex, England
[3] Uppsala Univ, Dept Genet & Pathol, S-75236 Uppsala, Sweden
[4] Uppsala Univ, Dept Genet & Dev, S-75236 Uppsala, Sweden
关键词
gene imprinting; transcription regulation; DNA-methylation; male germ cells; CTCF at 16q22; tumor suppressor; 16q22; LOH; BORIS at 20q13; oncogene; 20q13; amplification; cancer genetics and epigenetics;
D O I
10.1016/S1044-579X(02)00060-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CTCF is a ubiquitous 11 zinc finger (ZF) protein with highly versatile functions: in addition to transcriptional silencing or activating in a context-dependent fashion, it organizes epigenetically controlled chromatin insulators that regulate imprinted genes in soma. Recently, we have identified a CTCF paralogue, termed BORIS for Brother of the Regulator of Imprinted Sites, that is expressed only in the testis. BORIS has the same exons encoding the 11 ZF domain as mammalian CTCF genes, and hence interacts with similar cis elements, but encodes amino and carboxy termini distinct from those in CTCF. Normally, CTCF and BORIS are expressed in a mutually exclusive pattern that correlates with re-setting of methylation marks during male germ cell differentiation. The antagonistic features of these two gene siblings are underscored by showing that while CTCF overexpression blocks cell proliferation, expression of BORIS in normally BORIS-negative cells promotes cell growth which can lead to transformation. The suggestion that BORIS directs epigenetic reprogramming at CTCF target sites impinges on the observations that human BORIS is not only abnormally activated in a wide range of human cancers, but also maps to the cancer-associated amplification region at 20q13. The sibling rivalry occasioned by aberrant expression of BORIS in cancer may interfere with normal functions of CTCF including growth suppression, and contribute to epigenetic dysregulation which is a common feature in human cancer.
引用
收藏
页码:399 / 414
页数:16
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