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调节SM/J和NZB/BlNJ近交系小鼠磷脂转移活性的基因的数量性状基因座定位。

Quantitative trait locus mapping of genes that regulate phospholipid transfer activity in SM/J and NZB/BlNJ inbred mice.

作者信息

Korstanje Ron, Albers John J, Wolfbauer Gertrud, Li Renhua, Tu An-Yue, Churchill Gary A, Paigen Beverly J

机构信息

The Jackson Laboratory, Bar Harbor, ME, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2004 Jan;24(1):155-60. doi: 10.1161/01.ATV.0000104241.44819.10. Epub 2003 Oct 30.

Abstract

OBJECTIVE

Phospholipid transfer protein (PLTP), an important protein in the transfer of phospholipids between lipoprotein particles and in the remodeling of HDL, is regulated at both the transcriptional and the protein level. We performed quantitative trait locus (QTL) analysis to identify genomic loci regulating PLTP activity in mice.

METHODS AND RESULTS

Plasma PLTP activity was measured in 217 male F2 progeny from a SM/J x NZB/B1NJ intercross. Two QTL for plasma PLTP activity in mice fed chow (Pltpq1 and Pltpq2) were found on chromosomes 3 (34 cM, logarithm of odds [LOD] 3.5) and 10 (66 cM, LOD 4.1); two additional QTL in mice fed atherogenic diet (Pltpq3 and Pltpq4) were found on chromosomes 9 (56 cM, LOD 4.5) and 15 (34 cM, LOD 5.0); and one QTL (Pltiq1) for the inducibility of PLTP activity was found on chromosome 4 (70 cM, LOD 3.7). Several candidate genes for these 5 QTL were tested by sequence comparison and expression studies.

CONCLUSIONS

We identified five significant loci involved in PLTP activity in the mouse and provided supporting evidence for the candidacy of Nr1h4 and Apof as the genes underlying Pltpq2.

摘要

目的

磷脂转运蛋白(PLTP)是一种在脂蛋白颗粒间磷脂转运及高密度脂蛋白(HDL)重塑过程中起重要作用的蛋白质,其在转录水平和蛋白质水平均受到调控。我们进行了数量性状基因座(QTL)分析,以确定调控小鼠PLTP活性的基因组位点。

方法与结果

在来自SM/J×NZB/B1NJ杂交的217只雄性F2后代中测量血浆PLTP活性。在喂食普通饲料的小鼠中发现了两个血浆PLTP活性的QTL(Pltpq1和Pltpq2),分别位于3号染色体(34 cM,优势对数[LOD] 3.5)和10号染色体(66 cM,LOD 4.1);在喂食致动脉粥样化饮食的小鼠中又发现了另外两个QTL(Pltpq3和Pltpq4),分别位于9号染色体(56 cM,LOD 4.5)和15号染色体(34 cM,LOD 5.0);并且在4号染色体(70 cM,LOD 3.7)上发现了一个调控PLTP活性诱导性的QTL(Pltiq1)。通过序列比较和表达研究对这5个QTL的几个候选基因进行了检测。

结论

我们在小鼠中鉴定出了5个与PLTP活性相关的重要位点,并为Nr1h4和Apof作为Pltpq2潜在基因的候选资格提供了支持证据。

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