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首页> 外文期刊>Aquaculture Research >Microsatellite–centromere mapping in walking catfish Clarias macrocephalus (Günther, 1864) using gynogenetic diploids
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Microsatellite–centromere mapping in walking catfish Clarias macrocephalus (Günther, 1864) using gynogenetic diploids

机译:使用雌成虫二倍体对walking鱼小aria(Clarias macrocephalus,Günther,1864年)进行微卫星-着丝粒作图

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Thirty new microsatellite loci were isolated from a microsatellite-enriched genomic library of walking catfish Clarias macrocephalus. The CA motif was the most abundant, although several other motifs were also isolated. Two gynogenetic diploid families, each consisting of a female and 50 offspring, were genotyped at 56 microsatellite loci, including 30 loci developed in the present study and 26 loci reported in the previous study. Overall, 33 anonymous microsatellites derived from genomic library and 11 EST-linked microsatellites were mapped to their centromeres. High levels of chiasma interference were apparent in the walking catfish genome as indicated by an average frequency of second-division segregation (y) of 0.643 ± 0.248. Twenty-six loci (59%) showed a high microsatellite–centromere recombination, with a frequency >0.67, and three loci had recombination frequencies >0.9. This study demonstrated that gene–centromere mapping provided a rapid method for the expansion of the initial linkage map of walking catfish.
机译:从步行walking鱼Clarias macrocephalus的富含微卫星的基因组文库中分离出三十个新的微卫星基因座。尽管还分离了其他几个基元,但CA基元最丰富。在56个微卫星基因座上对两个雌激素发育二倍体家族进行了基因分型,其中包括本研究中开发的30个基因座和先前研究中报道的26个基因座。总体上,将33个来自基因组库的匿名微卫星和11个与EST相关的微卫星定位到了着丝粒。行走cat鱼基因组中明显出现了高水平的交叉干扰,其二次分裂的平均频率(y)为0.643±0.248。 26个基因座(59%)显示出高微卫星-着丝粒重组,频率> 0.67,三个基因座的重组频率> 0.9。这项研究表明,基因-着丝粒作图为扩大walking鱼的初始连锁作图提供了一种快速的方法。

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