Brown Lucia Y, Brown Stephen A
Columbia University College of Physicians and Surgeons, Department Obstetrics and Gynecology, Columbia University, 630 W 168th Street, New York, NY 10032, USA.
Trends Genet. 2004 Jan;20(1):51-8. doi: 10.1016/j.tig.2003.11.002.
Expansions of polyglutamine repeats are known to cause a variety of human neurodegenerative diseases. More recently, expansions of alanine tracts, particularly in transcription factor genes, have been shown to cause at least nine human conditions, including mental retardation and malformations of the brain, digits and other structures. Present knowledge suggests that alanine tract expansions generally, but not always, arise through unequal recombination as opposed to replication slippage, the most likely mechanism in other triplet repeat expansions. The function of alanine tracts is unknown but when alanine expansions occur in transcription factor genes, alanine tracts can result in either loss-of-function or gain of an abnormal function. Given the frequency of alanine tracts in proteins, it is likely that more alanine tract expansions will be discovered in disease genes.
已知聚谷氨酰胺重复序列的扩增会导致多种人类神经退行性疾病。最近,丙氨酸序列的扩增,尤其是转录因子基因中的扩增,已被证明会导致至少九种人类疾病,包括智力迟钝以及大脑、手指和其他结构的畸形。目前的知识表明,丙氨酸序列的扩增通常(但并非总是)通过不等交换产生,这与复制滑动相反,而复制滑动是其他三联体重复序列扩增中最可能的机制。丙氨酸序列的功能尚不清楚,但当丙氨酸扩增出现在转录因子基因中时,丙氨酸序列可能导致功能丧失或获得异常功能。鉴于蛋白质中丙氨酸序列的出现频率,很可能在疾病基因中会发现更多的丙氨酸序列扩增。