互补测试确定了恐惧相关行为的数量性状基因座的中介效应基因。

IF 11.1 Q1 CELL BIOLOGY Cell genomics Pub Date : 2024-05-08 Epub Date: 2024-05-01 DOI:10.1016/j.xgen.2024.100545
Patrick B Chen, Rachel Chen, Nathan LaPierre, Zeyuan Chen, Joel Mefford, Emilie Marcus, Matthew G Heffel, Daniela C Soto, Jason Ernst, Chongyuan Luo, Jonathan Flint
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引用次数: 0

摘要

了解参与数量性状的基因为了解行为的生物学基础提供了一个切入点,但从基因位点到行为变化的途径却鲜为人知。为了探索特定基因在恐惧行为中的作用,我们绘制了三个与恐惧相关的性状图,通过定量互补法测试了六个数量性状位点(QTL)上的十四个基因,并鉴定出六个基因。其中四个基因 Lamp、Ptprd、Nptx2 和 Sh3gl 在突触功能中具有已知的作用;第五个基因 Psip1 以前与行为无关;第六个基因 4933413L06Rik 是一个长非编码 RNA,功能未知。转录组和表观遗传模式的变异优先发生在兴奋性神经元中,这表明兴奋性神经元回路比抑制性神经元回路更允许遗传变异。我们的研究结果缓解了利用 QTL 遗传图谱揭示行为生物学基础的瓶颈,并促使人们重新考虑遗传变异与功能变异之间的预期关系。
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Complementation testing identifies genes mediating effects at quantitative trait loci underlying fear-related behavior.

Knowing the genes involved in quantitative traits provides an entry point to understanding the biological bases of behavior, but there are very few examples where the pathway from genetic locus to behavioral change is known. To explore the role of specific genes in fear behavior, we mapped three fear-related traits, tested fourteen genes at six quantitative trait loci (QTLs) by quantitative complementation, and identified six genes. Four genes, Lamp, Ptprd, Nptx2, and Sh3gl, have known roles in synapse function; the fifth, Psip1, was not previously implicated in behavior; and the sixth is a long non-coding RNA, 4933413L06Rik, of unknown function. Variation in transcriptome and epigenetic modalities occurred preferentially in excitatory neurons, suggesting that genetic variation is more permissible in excitatory than inhibitory neuronal circuits. Our results relieve a bottleneck in using genetic mapping of QTLs to uncover biology underlying behavior and prompt a reconsideration of expected relationships between genetic and functional variation.

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