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首页> 外文期刊>Behavior Genetics >The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language
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The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language

机译:芳香酶基因CYP19A1:几种遗传和功能的证据支持阅读,语音和语言中的作用

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Inspired by the localization, on 15q21.2 of the CYP19A1 gene in the linkage region of speech and language disorders, and a rare translocation in a dyslexic individual that was brought to our attention, we conducted a series of studies on the properties of CYP19A1 as a candidate gene for dyslexia and related conditions. The aromatase enzyme is a member of the cytochrome P450 super family, and it serves several key functions: it catalyzes the conversion of androgens into estrogens; during early mammalian development it controls the differentiation of specific brain areas (e.g. local estrogen synthesis in the hippocampus regulates synaptic plasticity and axonal growth); it is involved in sexual differentiation of the brain; and in songbirds and teleost fishes, it regulates vocalization. Our results suggest that variations in CYP19A1 are associated with dyslexia as a categorical trait and with quantitative measures of language and speech, such as reading, vocabulary, phonological processing and oral motor skills. Variations near the vicinity of its brain promoter region altered transcription factor binding, suggesting a regulatory role in CYP19A1 expression. CYP19A1 expression in human brain correlated with the expression of dyslexia susceptibility genes such as DYX1C1 and ROBO1. Aromatase-deficient mice displayed increased cortical neuronal density and occasional cortical heterotopias, also observed in Robo1−/− mice and human dyslexic brains, respectively. An aromatase inhibitor reduced dendritic growth in cultured rat neurons. From this broad set of evidence, we propose CYP19A1 as a candidate gene for human cognitive functions implicated in reading, speech and language.
机译:受本地化的启发,CYP19A1基因在语音和语言障碍的联系区域中的15q21.2位置,以及引起我们注意的阅读障碍患者中的​​罕见易位,我们对CYP19A1的特性进行了一系列研究阅读障碍和相关疾病的候选基因。芳香酶是细胞色素P450超级家族的成员,它具有几个关键功能:催化雄激素向雌激素的转化;在哺乳动物早期发育期间,它控制特定大脑区域的分化(例如,海马中的局部雌激素合成调节突触可塑性和轴突生长);它参与大脑的性别分化;在鸣禽和硬骨鱼类中,它调节发声。我们的研究结果表明,CYP19A1的变异与阅读障碍是一种分类特征,并且与语言和言语的定量测量有关,例如阅读,词汇,语音处理和口语运动技能。其大脑启动子区域附近的变异改变了转录因子的结合,提示在CYP19A1表达中起调节作用。 CYP19A1在人脑中的表达与阅读障碍易感基因如DYX1C1和ROBO1的表达相关。缺乏芳香酶的小鼠皮质神经元密度增加,偶有皮质异位症,在Robo1-/-小鼠和阅读障碍者的大脑中也分别观察到。芳香酶抑制剂减少了培养的大鼠神经元中的树突生长。从这些广泛的证据中,我们提出CYP19A1作为人类认知功能的候选基因,涉及阅读,语音和语言。

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