The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS(2018)

引用 4|浏览86
暂无评分
摘要
The presence of redundant copy number variants (CNVs) in groups of patients with neurological diseases suggests that these variants could have pathogenic effect. We have collected array CGH data of about 2.500 patients affected by neurocognitive disorders and we observed that CNVs in 2p16.3 locus were as frequent as those in 15q11.2, being both the most frequent unbalances in our cohort of patients. Focusing to 2p16.3 region, unbalances involving NRXN1 coding region have been already associated with neuropsychiatric disorders, although with incomplete penetrance, but little is known about CNVs located proximal to the gene. in the long noncoding RNA AK127244. We found that, in our cohort of patients with neuropsychiatric disorders. the frequency of CNVs involving AK127244 was comparable to that of NRXNI gene. Patients carrying 2p16.3 unbalances shared some common clinical characteristics regardless NRXNI and AK127244 CNVs localization. suggesting that the AK127244 long noncoding RNA could be involved in neurocognitive disease with the same effect of NRXNI unbalances. AK127244 as well as NRXNI unbalances seem to have a particular influence on language development, behavior or mood. according with the topographic correlation between NRXN1 expression and prefrontal cortex functions.
更多
查看译文
关键词
array CGH,CNVs,long noncoding RNA,NRXN1
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要