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Evolution of the alcohol dehydrogenase gene family in diploid and tetraploid Gossypium L.

机译:二倍体和四倍体棉L中酒精脱氢酶基因家族的演变

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Molecular data have had a profound effect on the field of plant evolutionary biology, yet the potential wealth of data stored in low-copy nuclear-encoded genes has been virtually ignored, relative to studies of chloroplast and ribosomal DNA. In this dissertation I present an analysis of a model nuclear-encoded gene family (alcohol dehydrogenase, Adh) in a model organismal system, the cotton genus (Gossypium L., Malvaceae).; A combination of PCR- and Southern hybridization-based approaches was employed to isolate, sequence, and map multiple Adh gene family members. Diploid Gossypium contain at least seven Adh loci. Sequence analysis reveals extensive intron variation between loci, and one locus has lost two introns. Evolutionary rates differ between loci and between lineages. Finally, the Adh gene family appears dynamic in that examples of gene duplication, pseudogenization, and elimination were found.; We have also employed Adh genes for phylogenetic analyses. We tested the relative utility of seven noncoding cpDNA regions and a pair of homoeologous nuclear genes for resolving recent divergences, using tetraploid cottons as a model system. We sequenced over 7 kb of CPDNA per taxon, yet obtained incomplete phylogenetic resolution. We also sequenced a 1.65-kb region of a homoeologous pair of Adh genes and obtained a robust and completely resolved topology. This enhanced resolution reflects an approximately three- to six-fold increase in evolutionary rate relative to the cpDNA sequences.; Finally we have exploited Adh sequences to study intraspecific genetic diversity. We estimated nucleotide diversity for a pair of homoeologous Adh loci in allotetraploid G. hirsutum. Nucleotide diversity for AdhA in Gossypium is lower than for any plant nuclear gene yet described. This low diversity appears to reflect a history severe genetic bottlenecks supplemented by an unusually slow nucleotide substitution rate and an autogamous breeding system. While not statistically supportable, the sum of the observations also suggest differential evolutionary dynamics at each of the homoeologous loci.
机译:分子数据对植物进化生物学领域产生了深远的影响,但是相对于叶绿体和核糖体DNA的研究,存储在低拷贝核编码基因中的潜在数据实际上被忽略了。在这篇论文中,我提出了一个模型生物系统,棉花属(棉属,锦葵科)中的模型核编码基因家族(酒精脱氢酶,Adh)的分析。基于PCR和Southern杂交的方法的组合用于分离,测序和定位多个Adh基因家族成员。二倍体棉包含至少七个Adh基因座。序列分析揭示了基因座之间广泛的内含子变异,一个基因座丢失了两个内含子。进化速率在基因座之间和谱系之间不同。最后,Adh基因家族似乎是动态的,因为发现了基因复制,假基因形成和消除的例子。我们还采用了Adh基因进行系统发育分析。我们使用四倍体棉作为模型系统,测试了七个非编码cpDNA区域和一对同源核基因在解决近期分歧方面的相对效用。我们对每个分类单元的7kb CPDNA进行了测序,但尚未获得完整的系统发育分辨率。我们还对Adh基因的同源对的1.65kb区域进行了测序,并获得了稳健且完全解析的拓扑。这种增强的分辨率反映了相对于cpDNA序列,进化速率大约提高了三到六倍。最后,我们利用Adh序列研究种内遗传多样性。我们估计了异源四倍体G. hirsutum中一对同源Adh基因座的核苷酸多样性。棉中AdhA的核苷酸多样性低于尚未描述的任何植物核基因。这种低多样性似乎反映了历史上严重的遗传瓶颈,辅以异常缓慢的核苷酸取代率和同卵繁殖系统。尽管没有统计依据,但观察结果的总和还表明每个同源位点的进化动力学都不同。

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