Corsi Ann K, Brodigan Thomas M, Jorgensen Erik M, Krause Michael
Department of Biology, The Catholic University of America, Washington, DC 20064, USA.
Development. 2002 Jun;129(11):2761-72. doi: 10.1242/dev.129.11.2761.
Twist is a transcription factor that is required for mesodermal cell fates in all animals studied to date. Mutations of this locus in humans have been identified as the cause of the craniofacial disorder Saethre-Chotzen syndrome. The Caenorhabditis elegans Twist homolog is required for the development of a subset of the mesoderm. A semidominant allele of the gene that codes for CeTwist, hlh-8, has defects that occur earlier in the mesodermal lineage than a previously studied null allele of the gene. The semidominant allele has a charge change (E29K) in the basic DNA-binding domain of CeTwist. Surprisingly, the mutant protein retains DNA-binding activity as both a homodimer and a heterodimer with its partner E/Daughterless (CeE/DA). However, the mutant protein blocks the activation of the promoter of a target gene. Therefore, the mutant CeTwist may cause cellular defects as a dominant negative protein by binding to target promoters as a homo- or heterodimer and then blocking transcription. Similar phenotypes as those caused by the E29K mutation were observed when amino acid substitutions in the DNA-binding domain that are associated with the human Saethre-Chotzen syndrome were engineered into the C. elegans protein. These data suggest that Saethre-Chotzen syndrome may be caused, in some cases, by dominant negative proteins, rather than by haploinsufficiency of the locus.
Twist是一种转录因子,在迄今为止所研究的所有动物中,它是中胚层细胞命运所必需的。人类中该基因座的突变已被确定为颅面疾病塞特雷-乔岑综合征的病因。秀丽隐杆线虫的Twist同源物是中胚层一个亚群发育所必需的。编码CeTwist的基因hlh-8的一个半显性等位基因,其缺陷出现在中胚层谱系中比该基因先前研究的无效等位基因更早的阶段。该半显性等位基因在CeTwist的碱性DNA结合结构域中有一个电荷变化(E29K)。令人惊讶的是,突变蛋白作为同二聚体以及与其伴侣E/无女儿基因(CeE/DA)形成的异二聚体都保留DNA结合活性。然而,突变蛋白会阻断靶基因启动子的激活。因此,突变的CeTwist可能作为一种显性负性蛋白,通过作为同二聚体或异二聚体与靶启动子结合,然后阻断转录,从而导致细胞缺陷。当将与人类塞特雷-乔岑综合征相关的DNA结合结构域中的氨基酸替换引入秀丽隐杆线虫蛋白时,观察到了与E29K突变引起的类似表型。这些数据表明,在某些情况下,塞特雷-乔岑综合征可能是由显性负性蛋白引起的,而不是由该基因座的单倍体不足引起的。