Ren J, Tang H, Yan X, Huang X, Zhang B, Ji H, Yang B, Milan D, Huang L
Key Laboratory for Animal Biotechnology of Jiangxi Province and the Ministry of Agriculture of China, Jiangxi Agricultural University, Nanchang, 330045, China.
J Anim Breed Genet. 2009 Feb;126(1):30-6. doi: 10.1111/j.1439-0388.2008.00751.x.
The enterotoxigenic Escherichia coli (ETEC) F4ac is a major cause of diarrhoea in newborn and young pigs. The locus for the intestinal ETEC F4ac receptor (F4acR) has been mapped to pig chromosome (SSC) 13q41 with known homology to human chromosome (HSA) 3q21 and q29. However, the causative gene and mutation(s) remain unknown. The aim of this study was to characterize gene-derived markers on SSC13q41 for fine mapping of the F4acR locus, and construct a high-resolution pig-human comparative map to select positional candidate genes for F4acR. Pig-specific sequence-tagged site markers were developed for 20 genes that are located in a 6.8-Mb region on HSA3q21 and q29, and a total of 34 single-nucleotide polymorphisms (SNPs) were identified in 14 of 20 markers developed. Eighteen markers were mapped to SSC13q41, while the other two markers (PLXNA1 and KLF15) were assigned to SSC13q32 and SSC7q13, respectively, by radiation hybrid mapping. This result showed that there was a small conserved segment on SSC7 corresponding to HSA3q21. A framework map comprising 18 markers on SSC13q41 was established, refining the synteny breakpoint on SSC13q41 to a region of 12.3 centiRay. The comparative radiation hybrid (RH) map revealed three interesting candidate genes for F4acR from the human genome, viz. MUC4, MUC13 and MUC20. Linkage analysis with six marker polymorphisms revealed that MUC4 had the most significant linkage with the F4acR locus.
产肠毒素大肠杆菌(ETEC)F4ac是新生仔猪和幼猪腹泻的主要病因。肠道ETEC F4ac受体(F4acR)基因座已定位到猪染色体(SSC)13q41,与人类染色体(HSA)3q21和q29具有已知的同源性。然而,致病基因和突变仍不清楚。本研究的目的是鉴定SSC13q41上的基因衍生标记,以精细定位F4acR基因座,并构建高分辨率的猪-人比较图谱,以选择F4acR的位置候选基因。针对位于HSA3q21和q29上6.8 Mb区域的20个基因开发了猪特异性序列标签位点标记,在开发的20个标记中的14个中总共鉴定出34个单核苷酸多态性(SNP)。通过辐射杂种图谱分析,18个标记被定位到SSC13q41,而另外两个标记(PLXNA1和KLF15)分别被定位到SSC13q32和SSC7q13。这一结果表明,SSC7上存在一个与HSA3q21相对应的小保守片段。建立了一个包含SSC13q41上18个标记的框架图谱,将SSC13q41上的同线性断点细化到12.3厘雷区域。比较辐射杂种(RH)图谱从人类基因组中揭示了三个有趣的F4acR候选基因,即MUC4、MUC13和MUC20。与六个标记多态性的连锁分析表明,MUC4与F4acR基因座的连锁最为显著。