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鉴定控制小鼠辐射诱导胸腺细胞凋亡水平的数量性状基因座。

Identification of quantitative trait loci controlling levels of radiation-induced thymocyte apoptosis in mice.

作者信息

Weil M M, Xia X, Lin Y, Stephens L C, Amos C I

机构信息

Department of Experimental Radiation Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, 77030-4095, USA.

出版信息

Genomics. 1997 Nov 1;45(3):626-8. doi: 10.1006/geno.1997.4999.

Abstract

Thymocyte apoptosis levels are higher in C57BL/6J mice than in C3Hf/Kam mice. Low-dose irradiation increases the numbers of thymocytes undergoing apoptosis, but the strain difference persists. We mapped three loci controlling radiation-induced thymocyte apoptosis levels in F2 intercross progeny of these strains. The strongest association of a genomic region with an apoptosis level occurred in a region of chromosome 11 known to harbor a locus (or loci) important in the pathogenesis of several rodent models of autoimmune disease. Additional loci influencing radiation-induced thymocyte apoptosis were identified on chromosomes 9 and 16. The genetic polymorphisms underlying these loci may have an evolutionary role in fine-tuning the apoptotic response in T cells and may be important in the etiology of lymphoproliferative disorders and autoimmunity.

摘要

C57BL/6J小鼠的胸腺细胞凋亡水平高于C3Hf/Kam小鼠。低剂量辐射会增加发生凋亡的胸腺细胞数量,但品系差异依然存在。我们在这些品系的F2代杂交后代中定位了三个控制辐射诱导胸腺细胞凋亡水平的基因座。基因组区域与凋亡水平之间最强的关联出现在11号染色体的一个区域,已知该区域含有一个(或多个)对几种自身免疫病啮齿动物模型发病机制很重要的基因座。在9号和16号染色体上还鉴定出了影响辐射诱导胸腺细胞凋亡的其他基因座。这些基因座潜在的遗传多态性可能在微调T细胞凋亡反应中具有进化作用,并且可能在淋巴增生性疾病和自身免疫病的病因学中具有重要意义。

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