Department of Obstetrics, Xiangya Hospital Central South University, 87 Xiangya Road, Changsha, 410008, China.
Hunan Engineering Research Center of Early Life Development and Disease Prevention, 87 Xiangya Road, Changsha, 410008, China.
Mol Neurobiol. 2021 Apr;58(4):1291-1302. doi: 10.1007/s12035-020-02193-w. Epub 2020 Nov 9.
Tubulin α-1 A (TUBA1A) mutations cause a wide spectrum of brain abnormalities. Although many mutations have been identified and functionally verified, there are clearly many more, and the relationship between TUBA1A mutations and brain malformations remains unclear. The aim of this study was to identify a TUBA1A mutation in a fetus with severe brain abnormalities, verify it functionally, and determine the mechanism of the mutation-related pathogenesis. A de novo missense mutation of the TUBA1A gene, c.167C>G p.T56R/P.THR56Arg, was identified by exon sequencing. Computer simulations showed that the mutation results in a disruption of lateral interactions between the microtubules. Transfection of 293T cells with TUBA1A p.T56R showed that the mutated protein is only partially incorporated into the microtubule network, resulting in a decrease in the rate of microtubule re-integration in comparison with the wild-type protein. The mechanism of pathological changes induced by the mutant gene was determined by knockdown and overexpression. It was found that knockdown of TUBA1A reduced the generation of neural progenitor cells, while overexpression of wild-type or mutant TUBA1A promoted neurogenesis. Our identification and functional verification of the novel TUBA1A mutation extends the TUBA1A gene-phenotype database. Loss-of-function of TUBA1A was shown to play an important role in early neurogenesis of TUBA1A mutation-related brain malformations.
微管蛋白 α-1A(TUBA1A)突变可导致广泛的脑异常。虽然已经鉴定和功能验证了许多突变,但显然还有更多的突变,并且 TUBA1A 突变与脑畸形之间的关系仍不清楚。本研究的目的是鉴定严重脑畸形胎儿的 TUBA1A 突变,对其进行功能验证,并确定突变相关发病机制的机制。通过外显子测序鉴定到 TUBA1A 基因的 c.167C>G p.T56R/P.THR56Arg 错义新生突变。计算机模拟表明,该突变导致微管之间的侧向相互作用中断。用 TUBA1A p.T56R 转染 293T 细胞后,发现突变蛋白仅部分掺入微管网络,与野生型蛋白相比,微管再整合的速度降低。通过敲低和过表达确定突变基因引起的病理变化的机制。结果发现,TUBA1A 的敲低降低了神经祖细胞的产生,而过表达野生型或突变型 TUBA1A 则促进了神经发生。我们对新型 TUBA1A 突变的鉴定和功能验证扩展了 TUBA1A 基因突变表型数据库。功能丧失性 TUBA1A 突变在 TUBA1A 突变相关脑畸形的早期神经发生中发挥重要作用。