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在具有ATF2犬直系同源基因错义突变的标准贵宾犬中出现的伴有癫痫发作的新生儿脑病。

A neonatal encephalopathy with seizures in standard poodle dogs with a missense mutation in the canine ortholog of ATF2.

作者信息

Chen Xuhua, Johnson Gary S, Schnabel Robert D, Taylor Jeremy F, Johnson Gayle C, Parker Heidi G, Patterson Edward E, Katz Martin L, Awano Tomoyuki, Khan Shahwanaz, O'Brien Dennis P

机构信息

Department of Veterinary Pathobiology, University of Missouri, 322 Connaway Hall, Columbia, MO, 65211, USA,

出版信息

Neurogenetics. 2008 Feb;9(1):41-9. doi: 10.1007/s10048-007-0112-2. Epub 2007 Dec 12.

Abstract

Neonatal encephalopathy with seizures (NEWS) is a previously undescribed autosomal recessive disease of standard poodle puppies. Affected puppies are small and weak at birth. Many die in their first week of life. Those surviving past 1 week develop ataxia, a whole-body tremor, and, by 4 to 6 weeks of age, severe generalized clonic-tonic seizures. None have survived to 7 weeks of age. Cerebella from affected puppies were reduced in size and often contained dysplastic foci consisting of clusters of intermixed granule and Purkinje neurons. We used deoxyribonucleic acid samples from related standard poodles to map the NEWS locus to a 2.87-Mb segment of CFA36, which contains the canine ortholog of ATF2. This gene encodes activating transcription factor 2 (ATF-2), which participates in the cellular responses to a wide variety of stimuli. We amplified and sequenced all coding regions of canine ATF2 from a NEWS-affected puppy and identified a T > G transversion that predicts a methionine-to-arginine missense mutation at amino acid position 51. Methionine-51 lies within a hydrophobic docking site for mitogen-activated protein kinases that activate ATF-2 so the arginine substitution is likely to interfere with ATF-2 activation. All 20 NEWS-affected puppies in the standard poodle family were homozygous for the mutant G allele. The 58 clinically normal family members were either G/T heterozygotes or homozygous for the ancestral T allele. There are no previous reports of spontaneous ATF2 mutations in people or animals; however, atf2-knockout mice have cerebellar lesions that are similar to those in puppies with NEWS.

摘要

新生儿癫痫性脑病(NEWS)是一种此前未被描述的标准贵宾犬幼犬常染色体隐性疾病。患病幼犬出生时体型小且虚弱。许多在出生后第一周内死亡。存活超过1周的幼犬会出现共济失调、全身震颤,到4至6周龄时会出现严重的全身性阵挛 - 强直发作。无一存活至7周龄。患病幼犬的小脑体积减小,且常含有发育异常灶,由混合的颗粒神经元和浦肯野神经元簇组成。我们使用来自相关标准贵宾犬的脱氧核糖核酸样本,将NEWS基因座定位到犬36号染色体(CFA36)上一个2.87兆碱基的片段,该片段包含ATF2的犬类直系同源基因。该基因编码激活转录因子2(ATF - 2),它参与细胞对多种刺激的反应。我们从一只受NEWS影响的幼犬中扩增并测序了犬ATF2的所有编码区,发现了一个T > G的颠换,预测在氨基酸位置51处有一个甲硫氨酸到精氨酸的错义突变。甲硫氨酸 - 51位于激活ATF - 2的丝裂原活化蛋白激酶的疏水对接位点内,因此精氨酸替代可能会干扰ATF - 2的激活。标准贵宾犬家族中所有20只受NEWS影响的幼犬均为突变G等位基因的纯合子。58名临床正常的家族成员要么是G/T杂合子,要么是祖先T等位基因的纯合子。此前没有关于人和动物中ATF2自发突变的报道;然而,敲除atf2基因的小鼠有与患NEWS的幼犬相似的小脑病变。

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