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Linkage Analysis of the Multilocus Glucosephosphate Isomerase Isozyme System in Sunfish (Centrarchidae Teleostii)

机译:翻车鱼(CentrarchidaeTeleostii)中多位点葡萄糖磷酸异构酶同工酶系统的连锁分析

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摘要

The purpose of the present investigation is to determine whether the two duplicated glucosephosphate isomerase (EC 5.3.1.9) loci Gpi-A and Gpi-B reside on the same chromosome in teleostean fishes. Interspecific sunfish hybrids were employed for the cross because of the different species-specific electrophoretic mobilities of the allelic isozymes at each GPI locus and because of their genomic compatibility. F1 sunfish hybrids, formed from a male warmouth (Lepomis gulosus) x female green sunfish (L. cyanellus) cross, were mated to form the F 2 generation. The number of each of the nine different isozyme phenotypes, revealed by starch gel electrophoresis, was determined using 256 F2 individuals. The high frequency of recombinant phenotypes in the F2 generation indicated that the two GPI loci are not linked. An excess of F 2 individuals heterozygous at both loci was observed and is interpreted as being caused by heterosis. The absence of linkage for the homologous loci encoding GPI subunits and for other multilocus isozyme systems is consistent with the postulate that the genomes of present-day vertebrates arose through one or more polyploidization events early in vertebrate evolution.
机译:本研究的目的是确定硬骨鱼类中两个重复的葡萄糖磷酸异构酶(EC 5.3.1.9)基因座Gpi-A和Gpi-B是否位于同一染色体上。种间sun鱼杂种被用于杂交,因为在每个GPI位点的等位基因同工酶具有不同的物种特异性电泳迁移率,并且由于它们的基因组相容性。由雄Warmouth(Lepomis gulosus)x雌性绿色Sunfish(L. cyanellus)杂交形成的F1太阳鱼杂种交配形成F 2代。通过256个F2个体确定了通过淀粉凝胶电泳揭示的9种不同同工酶表型的数目。 F2代中重组表型的高频率表明这两个GPI基因座没有联系。观察到在两个基因座上杂合子过量的F 2个体,并解释为由杂种优势引起。编码GPI亚基的同源基因座和其他多基因座同工酶系统没有连接,这与当今脊椎动物的基因组通过脊椎动物进化早期的一个或多个多倍化事件产生的假设相一致。

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