Biotech Research and Innovation Centre and Centre for Epigenetics, University of Copenhagen, Denmark.
Bioessays. 2012 Jan;34(1):50-60. doi: 10.1002/bies.201100107. Epub 2011 Oct 26.
The PRDM family has recently spawned considerable interest as it has been implicated in fundamental aspects of cellular differentiation and exhibits expanding ties to human diseases. The PRDMs belong to the SET domain family of histone methyltransferases, however, enzymatic activity has been determined for only few PRDMs suggesting that they act by recruiting co-factors or, more speculatively, confer methylation of non-histone targets. Several PRDM family members are deregulated in human diseases, most prominently in hematological malignancies and solid cancers, where they can act as both tumor suppressors or drivers of oncogenic processes. The molecular mechanisms have been delineated for only few PRDMs and little is known about functional redundancy within the family. Future studies should identify target genes of PRDM proteins and the protein complexes in which PRDM proteins reside to provide a more comprehensive understanding of the biological and biochemical functions of this important protein family.
PRDM 家族最近引起了相当大的兴趣,因为它与细胞分化的基本方面有关,并与人类疾病的联系不断扩大。PRDM 属于 SET 结构域组蛋白甲基转移酶家族,然而,只有少数 PRDM 的酶活性已被确定,这表明它们通过招募共因子起作用,或者更推测性地,赋予非组蛋白靶标的甲基化。几种 PRDM 家族成员在人类疾病中失调,在血液恶性肿瘤和实体瘤中最为明显,在这些疾病中,它们可以作为肿瘤抑制因子或致癌过程的驱动因子。只有少数 PRDM 的分子机制已经被描述,而且对于家族内的功能冗余知之甚少。未来的研究应该确定 PRDM 蛋白的靶基因和 PRDM 蛋白所在的蛋白质复合物,以更全面地了解这个重要蛋白家族的生物学和生物化学功能。