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SAMP6骨质疏松小鼠中的P518/Qrfp序列多态性

P518/Qrfp sequence polymorphisms in SAMP6 osteopenic mouse.

作者信息

Zhang Qing, Qiu Ping, Arreaza M Gladys, Simon Jason S, Golovko Andrei, Laverty Maureen, Vassileva Galya, Gustafson Eric L, Rojas-Triana Alberto, Bober Loretta A, Hedrick Joseph A, Monsma Frederick J, Greene Jonathan R, Bayne Marvin L, Murgolo Nicholas J

机构信息

Department of Discovery Technologies, Schering-Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA.

出版信息

Genomics. 2007 Nov;90(5):629-35. doi: 10.1016/j.ygeno.2007.07.011. Epub 2007 Sep 17.

Abstract

Mice lacking GPR103A expression display osteopenia. Analysis of mouse quantitative trait loci literature associated with bone mineral density suggested GPR103A ligand P518/Qrfp (chromosome 2qB) as a candidate osteoporosis gene. Promoter and coding regions of mouse P518/Qrfp were sequenced from genomic DNA obtained from the osteoporosis-prone strain SAMP6 and control strains SAMR1, A/J, AKR/J, BALB/c, C3H/HeJ, C57BL/6J, and DBA/2J. Four single-nucleotide polymorphisms (SNPs) were identified in only SAMP6 genomic DNA, g.-1773 T-->C, g.110 A-->G (N37S), g.188 G-->A (R63K), and g.135 T-->C (H45H). The promoter SNP generated a novel neuron-restrictive silencing factor binding site, a repressor that decreases gene expression in nonneuronal tissues. TaqMan analysis demonstrated fivefold lower P518/Qrfp liver expression in SAMP6 versus SAMR1 or C57BL/6J control strains. Tissue distribution of human, mouse, and rat P518/Qrfp and its receptors showed expression in bone and spinal cord. A direct role for P518/Qrfp function in maintaining bone mineral density is suggested.

摘要

缺乏GPR103A表达的小鼠表现出骨质减少。对与骨密度相关的小鼠数量性状基因座文献的分析表明,GPR103A配体P518/Qrfp(2号染色体qB)是一个候选骨质疏松症基因。从小鼠易患骨质疏松症的品系SAMP6以及对照品系SAMR1、A/J、AKR/J、BALB/c、C3H/HeJ、C57BL/6J和DBA/2J获得的基因组DNA中对小鼠P518/Qrfp的启动子和编码区进行测序。仅在SAMP6基因组DNA中鉴定出四个单核苷酸多态性(SNP),即g.-1773 T→C、g.110 A→G(N37S)、g.188 G→A(R63K)和g.135 T→C(H45H)。启动子SNP产生了一个新的神经元限制性沉默因子结合位点,该抑制因子可降低非神经元组织中的基因表达。TaqMan分析表明,与SAMR1或C57BL/6J对照品系相比,SAMP6中P518/Qrfp的肝脏表达降低了五倍。人、小鼠和大鼠P518/Qrfp及其受体的组织分布显示在骨骼和脊髓中有表达。提示P518/Qrfp功能在维持骨密度方面具有直接作用。

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