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在精神分裂症家族和同卵双胞胎中,没有CAG或GAA重复序列扩增的证据。

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins.

作者信息

Vincent J B, Kalsi G, Klempan T, Tatuch Y, Sherrington R P, Breschel T, McInnis M G, Brynjolfsson J, Petursson H, Gurling H M, Gottesman I I, Torrey E F, Petronis A, Kennedy J L

机构信息

Neurogenetics Section, Clarke Institute of Psychiatry, Toronto, Ontario, Canada.

出版信息

Hum Genet. 1998 Jul;103(1):41-7. doi: 10.1007/s004390050780.

Abstract

Many diseases caused by trinucleotide expansion exhibit increased severity and decreased age of onset (genetic anticipation) in successive generations. Apparent evidence of genetic anticipation in schizophrenia has led to a search for trinucleotide repeat expansions. We have used several techniques, including Southern blot hybridization, repeat expansion detection (RED) and locus-specific PCR to search for expanded CAG/CTG repeats in 12 families from the United Kingdom and 11 from Iceland that are multiplex for schizophrenia and demonstrate anticipation. The unstable DNA theory could also explain discordance of phenotype for schizophrenia in pairs of monozygotic twins, where the affected twin has a greater number of repeats than the unaffected twin. We used these techniques to look for evidence of different CAG/CTG repeat size in 27 pairs of monozygotic twins who are either concordant or discordant for schizophrenia. We have found no evidence of an increase in CAG/CTG repeat size for affected members in the families, or for the affected twins in the MZ twin sample. Southern hybridization and RED analysis were also performed for the twin and family samples to look for evidence of expansion of GAA/TTC repeats. However, no evidence of expansion was found in either sample. Whilst these results suggest that these repeats are not involved in the etiology of schizophrenia, the techniques used for detecting repeat expansions have limits to their sensitivity. The involvement of other trinucleotide repeats or other expandable repeat sequences cannot be ruled out.

摘要

许多由三核苷酸扩增引起的疾病在连续几代人中表现出病情加重和发病年龄降低(遗传早现)。精神分裂症中明显的遗传早现证据促使人们寻找三核苷酸重复扩增。我们使用了多种技术,包括Southern印迹杂交、重复序列扩增检测(RED)和位点特异性PCR,在来自英国的12个家庭和来自冰岛的11个家庭中寻找CAG/CTG重复序列的扩增,这些家庭患有精神分裂症且呈现遗传早现。不稳定DNA理论也可以解释同卵双胞胎中精神分裂症表型的不一致,其中患病双胞胎的重复序列数量比未患病双胞胎更多。我们使用这些技术在27对精神分裂症同卵双胞胎中寻找CAG/CTG重复序列大小不同的证据,这些双胞胎有的病情一致,有的不一致。我们没有发现这些家庭中患病成员或MZ双胞胎样本中患病双胞胎的CAG/CTG重复序列大小增加的证据。还对双胞胎和家庭样本进行了Southern杂交和RED分析,以寻找GAA/TTC重复序列扩增的证据。然而,在两个样本中均未发现扩增的证据。虽然这些结果表明这些重复序列不参与精神分裂症的病因,但用于检测重复序列扩增的技术在敏感性方面存在局限性。不能排除其他三核苷酸重复序列或其他可扩增重复序列的参与。

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