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猪6号染色体上碱性磷酸酶基因(ALPL)、烯醇化酶1(ENO1)、葡萄糖磷酸异构酶(GPI)、6-磷酸葡萄糖脱氢酶(PGD)和转化生长因子β1(TGFB1)之间的连锁关系。

Linkage relationships between ALPL, ENO1, GPI, PGD, and TGFB1 on porcine chromosome 6.

作者信息

Clamp P A, Feltes R, Shalhevet D, Beever J E, Atac E, Schook L B

机构信息

Department of Animal Sciences, University of Illinois, Urbana-Champaign.

出版信息

Genomics. 1993 Aug;17(2):324-9. doi: 10.1006/geno.1993.1328.

Abstract

A five-point linkage map has been established between the loci encoding liver/bone/kidney alkaline phosphatase (ALPL), enolase 1-alpha (ENO1), glucose-phosphate isomerase (GPI), phosphogluconate dehydrogenase (PGD), and transforming growth factor beta 1 (TGFB1) in swine. Linkage analysis was performed using the Meishan x Yorkshire three-generation reference pedigree at the University of Illinois (n = 91). Previously ENO1, GPI, PGD, and TGFB1 were mapped to porcine chromosome 6q by in situ hybridization but the linkage relations of TGFB1 and ENO1 with other loci in this group were not investigated. Based on mapping data from human chromosomes 1 and 19 and mouse chromosomes 4 and 7, it was postulated that ALPL should reside among or near these loci. Restriction fragment length polymorphisms were identified for ALPL, ENO1, and TGFB1. GPI (EC 5.3.1.9) and PGD (EC 1.1.1.44) phenotypes were determined by agarose gel electrophoresis of isozymes. Marker data were analyzed using the MLINK (two locus) and ILINK (multilocus) programs from LINKAGE (version 5.10). The most likely locus order between GPI-TGFB1-(PGD-ENO1)-ALPL with recombination rates of 0.049, 0.044, 0.000, and 0.156, respectively, could not be significantly determined. The maximum five-point lod score was the same to four decimal places irrespective of the order of ENO1 and PGD. This indicates that ENO1 and PGD are very closely linked and that ALPL is located telomeric to the established linkage group on pig chromosome 6.

摘要

已在猪中建立了一个五点连锁图谱,该图谱涉及编码肝/骨/肾碱性磷酸酶(ALPL)、烯醇化酶1-α(ENO1)、葡萄糖磷酸异构酶(GPI)、磷酸葡萄糖酸脱氢酶(PGD)和转化生长因子β1(TGFB1)的基因座。使用伊利诺伊大学的梅山猪×约克夏猪三代参考家系(n = 91)进行连锁分析。此前,ENO1、GPI、PGD和TGFB1通过原位杂交被定位到猪的6号染色体长臂,但未研究TGFB1和ENO1与该组中其他基因座的连锁关系。基于人类1号和19号染色体以及小鼠4号和7号染色体的定位数据,推测ALPL应位于这些基因座之中或附近。已鉴定出ALPL、ENO1和TGFB1的限制性片段长度多态性。通过同工酶的琼脂糖凝胶电泳确定GPI(EC 5.3.1.9)和PGD(EC 1.1.1.44)的表型。使用LINKAGE(版本5.10)中的MLINK(两个基因座)和ILINK(多个基因座)程序分析标记数据。GPI-TGFB1-(PGD-ENO1)-ALPL之间最可能的基因座顺序,其重组率分别为0.049、0.044、0.000和0.156,但无法显著确定。无论ENO1和PGD的顺序如何,最大五点lod分数在四位小数上是相同的。这表明ENO1和PGD紧密连锁,并且ALPL位于猪6号染色体上已建立的连锁群的端粒位置。

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