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本文引用的文献

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An updated systematic review of the role of host genetics in susceptibility to influenza.宿主遗传学在流感易感性中的作用的更新系统评价。
Influenza Other Respir Viruses. 2013 Sep;7 Suppl 2(Suppl 2):37-41. doi: 10.1111/irv.12079.
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Human G-proteins, ObgH1 and Mtg1, associate with the large mitochondrial ribosome subunit and are involved in translation and assembly of respiratory complexes.人类 G 蛋白 ObgH1 和 Mtg1 与大型线粒体核糖体亚基结合,并参与翻译和呼吸复合物的组装。
Nucleic Acids Res. 2013 Apr 1;41(6):3713-22. doi: 10.1093/nar/gkt079. Epub 2013 Feb 8.
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Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio.遗传关联表明,SMOC1 在产前性激素和指长比之间起中介作用。
Hum Genet. 2013 Apr;132(4):415-21. doi: 10.1007/s00439-012-1259-y. Epub 2012 Dec 22.
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Distinct gene loci control the host response to influenza H1N1 virus infection in a time-dependent manner.不同的基因座以时间依赖的方式控制宿主对 H1N1 流感病毒感染的反应。
BMC Genomics. 2012 Aug 20;13:411. doi: 10.1186/1471-2164-13-411.
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Junctate is a Ca2+-sensing structural component of Orai1 and stromal interaction molecule 1 (STIM1).连接蛋白是 Orai1 和基质相互作用分子 1(STIM1)的钙感应结构成分。
Proc Natl Acad Sci U S A. 2012 May 29;109(22):8682-7. doi: 10.1073/pnas.1200667109. Epub 2012 May 14.
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DOR/Tp53inp2 and Tp53inp1 constitute a metazoan gene family encoding dual regulators of autophagy and transcription.DOR/Tp53inp2 和 Tp53inp1 构成了一个后生动物基因家族,编码自噬和转录的双重调控因子。
PLoS One. 2012;7(3):e34034. doi: 10.1371/journal.pone.0034034. Epub 2012 Mar 28.
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Host genetics and Chlamydia disease: prediction and validation of disease severity mechanisms.宿主遗传学与衣原体病:疾病严重程度机制的预测与验证。
PLoS One. 2012;7(3):e33781. doi: 10.1371/journal.pone.0033781. Epub 2012 Mar 16.
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TP53INP1, a tumor suppressor, interacts with LC3 and ATG8-family proteins through the LC3-interacting region (LIR) and promotes autophagy-dependent cell death.TP53INP1,一种肿瘤抑制因子,通过 LC3 相互作用区域(LIR)与 LC3 和 ATG8 家族蛋白相互作用,并促进自噬依赖性细胞死亡。
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Association study of the single nucleotide polymorphisms of PARK2 and PACRG with leprosy susceptibility in Chinese population.中国人群中PARK2和PACRG单核苷酸多态性与麻风易感性的关联研究。
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Multigenic control and sex bias in host susceptibility to spore-induced pulmonary anthrax in mice.多基因控制和宿主对孢子诱导的小鼠肺炭疽易感性的性别偏向。
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肺炎型类鼻疽伯克霍尔德菌感染期间体重减轻的遗传控制。

Genetic control of weight loss during pneumonic Burkholderia pseudomallei infection.

作者信息

Emery Felicia D, Parvathareddy Jyothi, Pandey Ashutosh K, Cui Yan, Williams Robert W, Miller Mark A

机构信息

Department of Microbiology, Immunology & Biochemistry, The University of Tennessee Health Science Center, Memphis, TN, USA.

出版信息

Pathog Dis. 2014 Jul;71(2):249-64. doi: 10.1111/2049-632X.12172. Epub 2014 Apr 22.

DOI:10.1111/2049-632X.12172
PMID:24687986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4107055/
Abstract

Burkholderia pseudomallei (Bp) is the causal agent of a high-morbidity/mortality disease syndrome known as melioidosis. This syndrome can range from acute fulminate disease to chronic, local, and disseminated infections that are often difficult to treat because Bp exhibits resistance to many antibiotics. Bp is a prime candidate for use in biologic warfare/terrorism and is classified as a Tier-1 select agent by HHS and APHIS. It is known that inbred mouse strains display a range of susceptibility to Bp and that the murine infection model is ideal for studying acute melioidosis. Here, we exploit a powerful mouse genetics resource that consists of a large family of BXD-type recombinant inbred strains, to perform genome-wide linkage analysis of the weight loss phenotype following pneumonic infection with Bp. We infected parental mice and 32 BXD strains with 50-100 CFU of Bp (strain 1026b) and monitored weight retention each day over an eleven-day time course. Using the computational tools in GeneNetwork, we performed genome-wide linkage analysis to identify an interval on chromosome 12 that appears to control the weight retention trait. We then analyzed and ranked positional candidate genes in this interval, several of which have intriguing connections with innate immunity, calcium homeostasis, lipid transport, host cell growth and development, and autophagy.

摘要

类鼻疽伯克霍尔德菌(Bp)是一种被称为类鼻疽的高发病率/高死亡率疾病综合征的病原体。该综合征范围从急性暴发性疾病到慢性、局部和播散性感染,由于Bp对许多抗生素具有抗性,这些感染往往难以治疗。Bp是生物战/生物恐怖主义的主要候选病原体,被美国卫生与公众服务部(HHS)和美国动植物卫生检验局(APHIS)列为一级选择剂。已知近交系小鼠品系对Bp表现出一系列易感性,并且小鼠感染模型是研究急性类鼻疽的理想模型。在此,我们利用一个强大的小鼠遗传学资源,该资源由一大类BXD型重组近交系组成,对经Bp肺部感染后的体重减轻表型进行全基因组连锁分析。我们用50 - 100 CFU的Bp(菌株1026b)感染亲代小鼠和32个BXD品系,并在11天的时间过程中每天监测体重维持情况。使用基因网络中的计算工具进行全基因组连锁分析,以确定12号染色体上一个似乎控制体重维持性状的区间。然后我们分析并对该区间内的位置候选基因进行排序,其中几个基因与先天免疫、钙稳态、脂质转运、宿主细胞生长发育和自噬有着有趣的联系。