Packham Elizabeth A, Brook J David
Institute of Genetics, University of Nottingham, Queen's Medical Centre, Nottingham, NG7 2UH, UK.
Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R37-44. doi: 10.1093/hmg/ddg077.
The T-box gene family encodes a large family of transcription factors with more than 20 members identified in humans so far, and homologues in many other organisms. A number of human disorders have been linked to mutations in T-box genes, confirming their medical importance. They include Holt- Oram syndrome/TBX5, Ulnar-Mammary syndrome/TBX3, and more recently DiGeorge syndrome/TBX1, ACTH deficiency/TBX19 and cleft palate with ankyloglossia/TBX22. This review describes the key features of these disorders and the involvement of T-box genes in their phenotype.
T-box基因家族编码一大类转录因子,迄今为止在人类中已鉴定出20多个成员,在许多其他生物中也有同源物。许多人类疾病与T-box基因突变有关,证实了它们在医学上的重要性。这些疾病包括霍尔特-奥拉姆综合征/TBX5、尺骨-乳腺综合征/TBX3,以及最近发现的22q11.2缺失综合征/TBX1、促肾上腺皮质激素缺乏症/TBX19和伴有舌系带过短的腭裂/TBX22。本文综述了这些疾病的关键特征以及T-box基因在其表型中的作用。