Kidd J R, Matsubara Y, Castiglione C M, Tanaka K, Kidd K K
Department of Human Genetics, Yale University School of Medicine, New Haven, Connecticut 06510.
Genomics. 1990 Jan;6(1):89-93. doi: 10.1016/0888-7543(90)90451-y.
The gene for medium-chain acyl-CoA dehydrogenase (gene symbol ACADM; enzyme symbol MCAD) has been characterized for restriction fragment length polymorphisms (RFLPs) and mapped by linkage analysis to 4.2 cM from D1S2 and 11.7 cM from PGM1. The three RFLP systems described in detail show significant linkage disequilibrium but define four haplotypes with a PIC of 0.58. This makes ACADM informative for linkage mapping and for clinical genetic studies. By linkage studies, the orientation of these three loci relative to the centromere places ACADM most proximal. This is in direct conflict with the regional assignments of ACADM to 1p31 by in situ hybridization and of PGM1 to 1p22.1 by somatic cell studies. We suggest that this somatic cell localization of PGM1 may be incorrect.
中链酰基辅酶A脱氢酶基因(基因符号ACADM;酶符号MCAD)已针对限制性片段长度多态性(RFLP)进行了表征,并通过连锁分析定位到距D1S2 4.2厘摩和距PGM1 11.7厘摩处。详细描述的三种RFLP系统显示出显著的连锁不平衡,但定义了四个单倍型,多态信息含量(PIC)为0.58。这使得ACADM对连锁图谱构建和临床遗传学研究具有信息价值。通过连锁研究,这三个基因座相对于着丝粒的方向表明ACADM最靠近近端。这与通过原位杂交将ACADM定位于1p31以及通过体细胞研究将PGM1定位于1p22.1的区域定位直接冲突。我们认为PGM1的这种体细胞定位可能是错误的。