成人精品综合 I 黄色一及毛片 I 日本少妇裸体做爰高潮片 I 精品久久久久久中文字幕2017 I 全黄久久久久a级全毛片 I 国产精品资源一区二区 I 欧美巨大oooo I 999精品视频在线 I 中文精品在线观看 I 精品免费看国产一区二区 I 精品久久九九 I 亚洲国产成人精品青青草原 I 欧美女人天堂 I 成人亚洲a片v一区二区三区动漫 I 岛国一级 I 久久久免费毛片 I aaa少妇高潮大片免费看 I 好吊操精品视频 I 亚洲一区你懂的 I 国产精品1688网站

運動神經(jīng)元疾病“肌萎縮性脊髓側(cè)索硬化”（ALS）大約10%的病例是家族型的，但迄今所識別出的少量突變只占這些病例的20-30%左右?，F(xiàn)在，對來自攜帶ALS的家族的個體所做的一項新的研究，識別出了OPTN基因（編碼視神經(jīng)蛋白的基因）三種不同的、以前未知的突變。

OPTN早先被報道是罕見家族型青光眼的致病基因。視神經(jīng)蛋白抑制調(diào)控蛋白NF-κB的激發(fā)的能力在這些突變體中丟失了，說明NF-κB抑制因子在ALS治療中也許有用。

Mutations of optineurin in amyotrophic lateral sclerosis
Hirofumi Maruyama,Hiroyuki Morino,Hidefumi Ito,Yuishin Izumi,Hidemasa Kato,Yasuhito Watanabe,Yoshimi Kinoshita,Masaki Kamada,Hiroyuki Nodera,Hidenori Suzuki,Osamu Komure,Shinya Matsuura,Keitaro Kobatake,Nobutoshi Morimoto,Koji Abe,Naoki Suzuki,Masashi Aoki,Akihiro Kawata,Takeshi Hirai,Takeo Kato,Kazumasa Ogasawara,Asao Hirano,Toru Takumi,Hirofumi Kusaka,Koichi Hagiwara,
Ryuji Kaji & Hideshi Kawakami et al.

Amyotrophic lateral sclerosis （ALS） has its onset in middle age and is a progressive disorder characterized by degeneration of motor neurons of the primary motor cortex, brainstem and spinal cord1. Most cases of ALS are sporadic, but about 10% are familial. Genes known to cause classic familial ALS （FALS） are superoxide dismutase 1 （SOD1）2, ANG encoding angiogenin3, TARDP encoding transactive response （TAR） DNA-binding protein TDP-43 （ref. 4） and fused in sarcoma/translated in liposarcoma （FUS, also known as TLS）5, 6. However, these genetic defects occur in only about 20–30% of cases of FALS, and most genes causing FALS are unknown. Here we show that there are mutations in the gene encoding optineurin （OPTN）, earlier reported to be a causative gene of primary open-angle glaucoma （POAG）7, in patients with ALS. We found three types of mutation of OPTN: a homozygous deletion of exon 5, a homozygous Q398X nonsense mutation and a heterozygous E478G missense mutation within its ubiquitin-binding domain. Analysis of cell transfection showed that the nonsense and missense mutations of OPTN abolished the inhibition of activation of nuclear factor kappa B （NF-κB）, and the E478G mutation revealed a cytoplasmic distribution different from that of the wild type or a POAG mutation. A case with the E478G mutation showed OPTN-immunoreactive cytoplasmic inclusions. Furthermore, TDP-43- or SOD1-positive inclusions of sporadic and SOD1 cases of ALS were also noticeably immunolabelled by anti-OPTN antibodies. Our findings strongly suggest that OPTN is involved in the pathogenesis of ALS. They also indicate that NF-κB inhibitors could be used to treat ALS and that transgenic mice bearing various mutations of OPTN will be relevant in developing new drugs for this disorder.