IRCCS Associazione Oasi Institute for Research on Mental Retardation and Brain Aging, Troina, EN, Italy,
Neurol Sci. 2013 Nov;34(11):2023-5. doi: 10.1007/s10072-013-1529-z. Epub 2013 Aug 27.
Down's syndrome (DS) is the most frequent genetic cause of intellectual disability and is a chromosomal abnormality of chromosome 21 trisomy. The pericentrin gene (PCNT) has sequenced in 21q22.3 inside of the minimal critical region for Down's syndrome. Alterations of PCNT gene are associated with dwarfism, cardiomyopathy and other pathologies. In this study, we have evaluated the possible differential expression of PCNT mRNA, by qRT-PCR, in peripheral blood leukocytes of DS subjects compared with the normal population. In the present case-control study, PCNT gene expression was increased by 72.72% in 16 out 22 DS samples compared with normal subjects. Our data suggest that changes in the expression levels of PCNT in DS subjects may be involved into the molecular mechanism of Down's syndrome.
唐氏综合征(DS)是最常见的智力障碍的遗传原因,是 21 号染色体三体的染色体异常。中心体蛋白基因(PCNT)已在唐氏综合征最小关键区域的 21q22.3 内测序。PCNT 基因突变与矮身材、心肌病和其他病理有关。在这项研究中,我们通过 qRT-PCR 评估了外周血白细胞中 PCNT mRNA 在 DS 患者与正常人群中的可能差异表达。在本病例对照研究中,与正常对照组相比,22 例 DS 样本中有 16 例的 PCNT 基因表达增加了 72.72%。我们的数据表明,DS 患者 PCNT 表达水平的变化可能参与唐氏综合征的分子机制。