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首页> 外文期刊>The European Journal of Neuroscience >Identification of a Chr 11 quantitative trait locus that modulates proliferation in the rostral migratory stream of the adult mouse brain.
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Identification of a Chr 11 quantitative trait locus that modulates proliferation in the rostral migratory stream of the adult mouse brain.

机译:Chr 11定量性状基因座的鉴定,该基因座可调节成年小鼠大脑的有角迁移流中的增殖。

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Neuron production takes place continuously in the rostral migratory stream (RMS) of the adult mammalian brain. The molecular mechanisms that regulate progenitor cell division and differentiation in the RMS remain largely unknown. Here, we surveyed the mouse genome in an unbiased manner to identify candidate gene loci that regulate proliferation in the adult RMS. We quantified neurogenesis in adult C57BL/6J and A/J mice, and 27 recombinant inbred lines derived from those parental strains. We showed that the A/J RMS had greater numbers of bromodeoxyuridine-labeled cells than that of C57BL/6J mice with similar cell cycle parameters, indicating that the differences in the number of bromodeoxyuridine-positive cells reflected the number of proliferating cells between the strains. AXB and BXA recombinant inbred strains demonstrated even greater variation in the numbers of proliferating cells. Genome-wide mapping of this trait revealed that chromosome 11 harbors a significant quantitative trait locus at 116.75 +/- 0.75 Mb that affects cell proliferation in the adult RMS. The genomic regions that influence RMS proliferation did not overlap with genomic regions regulating proliferation in the adult subgranular zone of the hippocampal dentate gyrus. On the contrary, a different, suggestive locus that modulates cell proliferation in the subgranular zone was mapped to chromosome 3 at 102 +/- 7 Mb. A subset of genes in the chromosome 11 quantitative trait locus region is associated with neurogenesis and cell proliferation. Our findings provide new insights into the genetic control of neural proliferation and an excellent starting point to identify genes critical to this process.
机译:在成年哺乳动物脑的延髓迁徙流(RMS)中,神经元的产生持续进行。在RMS中调节祖细胞分裂和分化的分子机制仍然未知。在这里,我们以无偏见的方式调查了小鼠基因组,以确定调节成年RMS中增殖的候选基因位点。我们量化了成年C57BL / 6J和A / J小鼠和从这些亲本菌株衍生的27个重组自交系的神经发生。我们显示,与具有相似细胞周期参数的C57BL / 6J小鼠相比,A / J RMS的溴脱氧尿苷标记的细胞数量更多,这表明溴脱氧尿苷阳性细胞数量的差异反映了菌株之间增殖细胞的数量。 AXB和BXA重组近交菌株在增殖细胞数量方面表现出更大的差异。该性状的全基因组分布图揭示,第11号染色体在116.75 +/- 0.75 Mb处具有重要的定量性状基因座,影响成年RMS中的细胞增殖。影响RMS增殖的基因组区域与调节海马齿状回的成年亚颗粒区的增殖的基因组区域不重叠。相反,另一种暗示性基因座可调节亚颗粒区的细胞增殖,并定位在102 +/- 7 Mb的3号染色体上。 11号染色体定量性状基因座区域中的基因子集与神经发生和细胞增殖有关。我们的发现为神经增殖的遗传控制提供了新的见识,并为确定对该过程至关重要的基因提供了一个很好的起点。

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