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Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction.脊髓性肌萎缩症:从snRNP组装的伴侣蛋白缺陷到神经肌肉功能障碍
Front Mol Biosci. 2017 Jun 8;4:41. doi: 10.3389/fmolb.2017.00041. eCollection 2017.
2
Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans.局部性的TWIST1和TWIST2碱性结构域替换会引发四种不同的人类疾病,这些疾病可以在秀丽隐杆线虫中建模。
Hum Mol Genet. 2017 Jun 1;26(11):2118-2132. doi: 10.1093/hmg/ddx107.
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Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis.神经钙蛋白δ抑制通过恢复受损的内吞作用,对人类及跨物种的脊髓性肌萎缩起到保护作用。
Am J Hum Genet. 2017 Feb 2;100(2):297-315. doi: 10.1016/j.ajhg.2017.01.005. Epub 2017 Jan 26.
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CRISPR gene-editing tested in a person for the first time.CRISPR基因编辑首次在人体中进行测试。
Nature. 2016 Nov 24;539(7630):479. doi: 10.1038/nature.2016.20988.
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Small molecule stabilization of the KSR inactive state antagonizes oncogenic Ras signalling.KSR非活性状态的小分子稳定作用可拮抗致癌性Ras信号传导。
Nature. 2016 Sep 1;537(7618):112-116. doi: 10.1038/nature19327. Epub 2016 Aug 24.
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Chinese scientists to pioneer first human CRISPR trial.中国科学家将率先开展首次人体CRISPR试验。
Nature. 2016 Jul 28;535(7613):476-7. doi: 10.1038/nature.2016.20302.
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Decreased function of survival motor neuron protein impairs endocytic pathways.存活运动神经元蛋白功能降低会损害内吞途径。
Proc Natl Acad Sci U S A. 2016 Jul 26;113(30):E4377-86. doi: 10.1073/pnas.1600015113. Epub 2016 Jul 11.
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Less Is More: Substrate Reduction Therapy for Lysosomal Storage Disorders.少即是多:溶酶体贮积症的底物减少疗法
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Barber-Say syndrome and Ablepharon-Macrostomia syndrome: An overview.巴伯-赛伊综合征和无睑-大口畸形综合征:综述。
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10
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.分析 589306 个人的基因组,确定对严重孟德尔儿童疾病有抵抗力的个体。
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从表型相似基因到沉默抑制因子:确定人类疾病的潜在治疗靶点。

From phenologs to silent suppressors: Identifying potential therapeutic targets for human disease.

作者信息

Golden Andy

机构信息

Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

出版信息

Mol Reprod Dev. 2017 Nov;84(11):1118-1132. doi: 10.1002/mrd.22880. Epub 2017 Oct 3.

DOI:10.1002/mrd.22880
PMID:28834577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5690827/
Abstract

Orthologous phenotypes, or phenologs, are seemingly unrelated phenotypes generated by mutations in a conserved set of genes. Phenologs have been widely observed and accepted by those who study model organisms, and allow one to study a set of genes in a model organism to learn more about the function of those genes in other organisms, including humans. At the cellular and molecular level, these conserved genes likely function in a very similar mode, but are doing so in different tissues or cell types and can result in different phenotypic effects. For example, the RAS-RAF-MEK-MAPK pathway in animals is a highly conserved signaling pathway that animals adopted for numerous biological processes, such as vulval induction in Caenorhabditis elegans and cell proliferation in mammalian cells; but this same gene set has been co-opted to function in a variety of cellular contexts. In this review, I give a few examples of how suppressor screens in model organisms (with a emphasis on C. elegans) can identify new genes that function in a conserved pathway in many other organisms. I also demonstrate how the identification of such genes can lead to important insights into mammalian biology. From such screens, an occasional silent suppressor that does not cause a phenotype on its own is found; such suppressors thus make for good candidates as therapeutic targets.

摘要

直系同源表型,或表型同源物,是由一组保守基因中的突变产生的看似不相关的表型。表型同源物已被研究模式生物的人员广泛观察到并接受,它使人们能够在模式生物中研究一组基因,以更多地了解这些基因在包括人类在内的其他生物中的功能。在细胞和分子水平上,这些保守基因可能以非常相似的方式发挥作用,但在不同的组织或细胞类型中发挥作用,并可能导致不同的表型效应。例如,动物中的RAS-RAF-MEK-MAPK途径是一条高度保守的信号通路,动物将其用于许多生物学过程,如秀丽隐杆线虫的外阴诱导和哺乳动物细胞的细胞增殖;但这同一组基因已被用于多种细胞环境中发挥作用。在这篇综述中,我给出了一些例子,说明模式生物(重点是秀丽隐杆线虫)中的抑制子筛选如何能够识别在许多其他生物中保守途径中发挥作用的新基因。我还展示了识别此类基因如何能够对哺乳动物生物学产生重要见解。通过此类筛选,偶尔会发现一种自身不会导致表型的沉默抑制子;因此,此类抑制子是很好的治疗靶点候选物。