Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-3403, USA.
Physiol Genomics. 2010 Sep;42A(1):1-7. doi: 10.1152/physiolgenomics.00096.2010. Epub 2010 Jun 22.
To confirm seizure susceptibility (SZS) quantitative trait loci (QTLs) on chromosome (chr) 15 identified previously using C57BL/6J (B6) and DBA/2J (D2) mice and to refine their genomic map position, we studied a set of three congenic strains in which overlapping segments of chr 15 from D2 were transferred onto the B6 background. We measured thresholds for generalized electroshock seizure (GEST) and maximal electroshock seizure (MEST) in congenic strains and B6-like littermates and also tested their responses to kainic acid (KA) and pentylenetetrazol (PTZ). Results document that MEST is significantly lower in strains 15M and 15D, which harbor medial and distal (telomeric) segments of chr 15 (respectively) from D2, compared with strain 15P, which harbors the proximal (acromeric) segment of chr 15 from D2, and with control littermates. Congenic strains 15P and 15M exhibited greater KA SZS compared with strain 15D and B6-like controls. All congenic strains were similar to controls with regard to PTZ SZS. Taken together, results suggest there are multiple SZS QTLs on chr 15 and that two QTLs harbor gene variants that affect MEST and KA SZS independently. The MEST QTL is refined to a 19 Mb region flanked by rs13482630 and D15Mit159. This interval contains 350 genes, 183 of which reside in areas where the polymorphism rate between B6 and D2 is high. The KA QTL interval spans a 65 Mb region flanked by markers D15Mit13 and rs31271969. It harbors 83 genes in highly polymorphic areas, 310 genes in all. Complete dissection of these loci will lead to identification of genetic variants that influence SZS in mice and provide a better understanding of seizure biology.
为了确认先前使用 C57BL/6J(B6)和 DBA/2J(D2)小鼠在 15 号染色体(chr)上鉴定出的癫痫易感性(SZS)数量性状基因座(QTL),并精确定位其基因组图谱位置,我们研究了一组三个在 B6 背景上重叠来自 D2 的 chr15 片段的同系繁殖株系。我们测量了同系繁殖株系和 B6 类似品系的广义电休克癫痫发作(GEST)和最大电休克癫痫发作(MEST)的阈值,并且还测试了它们对海人酸(KA)和戊四氮(PTZ)的反应。结果表明,与携带 D2 近端(端粒)chr15 片段的 15P 株系和对照品系相比,15M 和 15D 株系的 MEST 明显更低,而 15D 株系携带 D2 中的 chr15 中间和远端(端粒)片段,15P 和 15M 株系的 KA SZS 比 15D 株系和 B6 类似对照品系更高。所有同系繁殖株系在 PTZ SZS 方面与对照品系相似。总之,结果表明,chr15 上存在多个 SZS QTL,并且两个 QTL 携带影响 MEST 和 KA SZS 的独立基因变异体。MEST QTL 被细化到一个 19 Mb 的区域,由 rs13482630 和 D15Mit159 侧翼。该区间包含 350 个基因,其中 183 个位于 B6 和 D2 之间多态性率较高的区域。KA QTL 区间跨越由标记 D15Mit13 和 rs31271969 侧翼的 65 Mb 区域。它在高度多态性区域内包含 83 个基因,在所有区域内包含 310 个基因。对这些基因座的完全剖析将导致鉴定影响小鼠 SZS 的遗传变异体,并更好地了解癫痫生物学。