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Researchers Identify Gene That Leads to Myopia

ScienceDaily (Sep. 2, 2011) — A Ben-Gurion University of the Negev research group led by Prof. Ohad Birk has identified a gene whose defect specifically causes myopia or nearsightedness.


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See Also:
Health & Medicine
•Eye Care
•Genes
•Gene Therapy
•Human Biology
ersonalized Medicine
•Birth Defects
Reference
•Vitreous humour
•Myopia
•Refractive surgery
•Hyperopia
In an article appearing online in the American Journal of Human Genetics, Birk and his team reveal that a mutation in LEPREL1 has been shown to cause myopia.

"We are finally beginning to understand at a molecular level why nearsightedness occurs," Prof. Birk says. The discovery was a group effort at BGU's Morris Kahn Laboratory of Human Genetics at the National Institute for Biotechnology in the Negev and the Dayan Clinical Genetics Wing at Soroka University Medical Center.

Nearsightedness is the most common human eye disorder and is mostly a hereditary trait. Aside from being a significant public health concern, nearsightedness also leads to a higher incidence of other secondary eye disorders, such as retinal detachment, macular degeneration, as well as early onset glaucoma and cataracts. Despite decades of intensive research, the specific genes whose defects lead to nearsightedness have remained elusive.

The defective gene was identified in a thorough study of severe early-onset myopia that is common in a specific Bedouin tribe in southern Israel. As part of the research and in collaboration with a Finnish group, studies in a model system using insect cells demonstrated that the mutation is detrimental to the enzymatic activity of the gene.

The gene, LEPREL1, encodes an enzyme that is essential for the final modification of collagen in the eye. In the absence of the active form of this enzyme, aberrant collagen is formed, causing the human eyeball to be longer than normal. As a consequence, light beams entering the eyeball focus in front of the retina rather than on the retina itself and myopia emerges.

Future studies will determine whether LEPREL1 or its related genes play a significant role in the causation of myopia in the population at large as well.

Prof. Birk's group has thus far elucidated the molecular mechanisms leading to more than 15 human diseases, and the research findings are effectively implemented in massive screening tests and prevention programs.
多认识些朋友。。。。
多认识些朋友。。。。
日科学(2011年9月2,) - 本 - 古里安大学的内盖夫Ohad Birk教授领导的研究小组发现了一种基因,其缺陷,特别是造成近视或近视。


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另请参见:
医药卫生
•眼部护理
•基因
•基因疗法
•人类生物学
•ersonalized医药
•出生缺陷
参考
•玻璃体
•近视
•屈光手术
•远视
在一篇文章中出现的美国人类遗传学,Birk和他的团队杂志“网上透露,在LEPREL1突变已被证明是造成近视。
“我们终于开始明白为什么近视发生在分子水平上,”Birk教授说。这一发现是在BGU的莫里斯卡恩在国家生物技术在内盖夫沙和大雁索罗卡大学医学中心的临床遗传学荣研究所的人类遗传学实验室的集团努力。
近视是人类最常见的眼部疾病,主要是一种遗传性状。除了作为一个重要的公共卫生问题,近视的其他次要眼疾,如视网膜脱离,黄斑变性,以及发病早期青光眼和白内障的发病率较高,也导致。尽管几十年的深入研究特定基因的缺陷导致近视仍然难以实现。
在深入研究了严重的早发性近视,是在一个特定的贝都因人在以色列南部的部落共同缺陷的基因被确定。作为研究的一部分,并在与芬兰的一个组合作,在一个模型系统研究表明,利用昆虫细胞酶活性的基因突变是有害的。
,LEPREL1,基因编码一种酶,是必不可少的胶原蛋白眼的最后修改。在缺乏这种酶的活性形式,异常的胶原蛋白形成,造***类眼球比正常情况下更长的时间。因此,光束进入眼球的焦点,在视网膜的前面,而不是本身和近视出现在视网膜上。
未来的研究将确定是否LEPREL1或与其有关的基因在近视的因果关系发挥了显著作用,在人口以及大。
Birk教授的研究小组迄今已阐明了导致人类疾病的超过15的分子机制,以及研究结果是有效地在大量的筛选试验和预防方案的实施。
生命不息,战斗不止。
谢谢凤凰涅槃的翻译
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