Semenza G L
Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-3914.
Hum Mutat. 1994;3(3):180-99. doi: 10.1002/humu.1380030304.
Transcription factors are key mediators of the genetic programs that underlie human development and physiology. Mutations in genes that encode transcription factors or in DNA sequences to which these factors bind may adversely affect gene expression and result in disease. Mutations in genes encoding transcription factors often have pleiotropic effects because each transcription factor is involved in the regulation of multiple genes. For several transcription factors, germline mutations have been shown to result in malformation syndromes whereas somatic mutations in the same genes contribute to the multistep process of tumorigenesis. The study of transcription factors and their involvement in human disease thus provides insight into the molecular mechanisms underlying human development, physiology, dysmorphology, and oncology.
转录因子是构成人类发育和生理基础的遗传程序的关键调节因子。编码转录因子的基因或这些因子所结合的DNA序列发生突变,可能会对基因表达产生不利影响并导致疾病。编码转录因子的基因突变通常具有多效性,因为每个转录因子都参与多个基因的调控。对于几种转录因子而言,种系突变已被证明会导致畸形综合征,而同一基因中的体细胞突变则促成肿瘤发生的多步骤过程。因此,对转录因子及其在人类疾病中的作用进行研究,有助于深入了解人类发育、生理、畸形学和肿瘤学背后的分子机制。