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对大鼠重组近交系HXB/BXH组进行基因组扫描,以寻找与条件性味觉厌恶相关的数量性状基因座。

Genome scanning of the HXB/BXH sets of recombinant inbred strains of the rat for quantitative trait loci associated with conditioned taste aversion.

作者信息

Bielavská Edita, Kren Vladimir, Musilová Alena, Zídek Václav, Pravenec Michal

机构信息

Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic.

出版信息

Behav Genet. 2002 Jan;32(1):51-6. doi: 10.1023/a:1014407928865.

Abstract

In the current study, we searched for quantitative trait loci (QTL) responsible for a conditioned taste aversion (CTA) measured as a decrease in the intake of a saccharin conditioned stimulus followed by an i.p. injection of 0.15 M LiCl (lithium chloride) (2 ml/100 g body weight). A genome scanning for QTL associated with CTA was performed in the HXB/BXH sets of recombinant inbred (RI) strains derived from the Brown Norway (BN-Lx) rat and the spontaneously hypertensive rat (SHR). The BN-Lx progenitor showed a significantly stronger CTA (8.3+/-2.8%) than the SHR progenitor (27.8+/-3.3%, p < .0001). The distribution of CTA values among RI strains was continuous, suggesting a polygenic mode of inheritance. Genome scanning of RI strains with more than 700 gene markers revealed a significant association of CTA with the D2Cebr11s4 marker on chromosome 2 (LRS = 22.7) and with the D4Cebrp149s8 marker on chromosome 4 (LRS = 23.4). The chromosome 2 putative QTL was confirmed by detecting a significant difference in CTA between the SHR progenitor (27.8+/-3.3%) and the SHR-2 (SHR.BN-D2Rat171/D2Arb24) congenic strain (13.1+/-4.4%, p < .01) that are genetically identical except for a segment of chromosome 2 that was transferred onto the genetic background of the SHR from the BN strain.

摘要

在当前研究中,我们寻找与条件性味觉厌恶(CTA)相关的数量性状基因座(QTL),CTA通过糖精条件刺激物摄入量的减少来衡量,随后腹腔注射0.15M氯化锂(LiCl)(2ml/100g体重)。在源自布朗挪威大鼠(BN-Lx)和自发性高血压大鼠(SHR)的重组近交(RI)品系的HXB/BXH组中进行了与CTA相关的QTL的全基因组扫描。BN-Lx祖代显示出比SHR祖代更强的CTA(8.3±2.8%)(27.8±3.3%,p<.0001)。RI品系中CTA值的分布是连续的,表明其遗传模式为多基因遗传。对具有700多个基因标记的RI品系进行全基因组扫描,发现CTA与2号染色体上的D2Cebr11s4标记(LRS=22.7)以及4号染色体上的D4Cebrp149s8标记(LRS=23.4)存在显著关联。通过检测SHR祖代(27.8±3.3%)和SHR-2(SHR.BN-D2Rat171/D2Arb24)同源基因品系(13.1±4.4%,p<.01)之间CTA的显著差异,证实了2号染色体上的假定QTL,这两个品系除了从BN品系转移到SHR遗传背景上的2号染色体片段外,基因完全相同。

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