首页> 外文期刊>Cellular & molecular biology letters. >Intraspecific polymorphism of ribosomal DNA loci number and morphology in Brachypodium pinnatum and Brachypodium sylvaticum.
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Intraspecific polymorphism of ribosomal DNA loci number and morphology in Brachypodium pinnatum and Brachypodium sylvaticum.

机译:短枝短孢菌和西短枝短螺旋体核糖体DNA基因座数的种内多态性和形态。

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The genus Brachypodium has become the target of extensive cytomolecular studies since one of its representatives, B. distachyon, has been accepted as a model plant for temperate cereals and forage grasses. Recent preliminary studies suggested that intraspecific rDNA polymorphism can occur in at least two members of the genus, B. sylvaticum and B. pinnatum, so the aim of this study was to further analyse this phenomenon. FISH with 25S rDNA and 5S rDNA probes was performed on somatic metaphase chromosomes, supplemented by the silver staining technique which distinguishes transcriptionally active from inactive 18S-5.8S-25S rDNA loci. The number, size and chromosomal distribution of 5S rDNA loci were very constant: two loci were invariably observed in all studied diploid accessions of both species, while four 5S rDNA loci were present in the tetraploid B. pinnatum. In contrast to 5S rDNA loci, those of the 35S rDNA were more variable. Two or three loci were observed in the diploid B. pinnatum and four in tetraploid accessions. In chromosome complements of B. sylvaticum accessions from two to six 35S rDNA sites were detected. Regardless of total rDNA locus number, only two were transcriptionally active in diploid accessions of both species, while two or four were active in the tetraploid B. pinnatum. Additionally, the fluorescent CMA/DAPI banding method was used to identify the relation between rDNA sites and CMA+ bands. It was revealed that the number and chromosomal distribution of CMA+ bands are in congruence only with 35S rDNA loci which gave strong FISH signals.
机译:自从其代表之一B.distachyon已被接受为温带谷物和牧草的典范植物以来,Brachypodium属已成为广泛的细胞分子研究的目标。最近的初步研究表明,种内rDNA多态性可以在至少两个属中发生,即S.vaylum和B.pinnatum,因此本研究的目的是进一步分析这种现象。在体细胞中期染色体上用25S rDNA和5S rDNA探针进行FISH,辅之以银染技术,该技术可将转录活性和非活性18S-5.8S-25S rDNA基因座区分开。 5S rDNA基因座的数量,大小和染色体分布非常恒定:在两个物种的所有研究二倍体种质中始终观察到两个基因座,而四倍体B. pinnatum中存在四个5S rDNA基因座。与5S rDNA基因座相反,35S rDNA基因座的可变性更大。在二倍体B. pinnatum中观察到两个或三个基因座,在四倍体中观察到四个基因座。在S.vaylum B. sylvaticum的染色体补体中,检测到两个至六个35S rDNA位点。不论总rDNA基因座数目如何,两个物种在二倍体种中只有两个具有转录活性,而在四倍体B. pinnatum中有两个或四个具有转录活性。此外,荧光CMA / DAPI谱带法用于鉴定rDNA位点与CMA +谱带之间的关系。结果表明,CMA +条带的数目和染色体分布仅与35S rDNA基因座一致,后者给出了很强的FISH信号。

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