荧光原位杂交技术检测苹果核糖体RNA基因

Masashi Yamamoto, S. Moriya, Toshiya Yamamoto
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引用次数: 1

摘要

采用荧光原位杂交技术(FISH)测定了苹果‘Sensyu’(Malus × domestica Borkh.)开放授粉幼苗染色体上18S-5.8S-25S和5S核糖体RNA基因(rnas)的位置。用生物素标记18S-5.8S-25S和5S rDNA探针,在DAPI反染的染色体上用异硫氰酸荧光素(FITC)-亲和素偶联物检测杂交信号。在34条染色体的端粒位置检测到18S-5.8S-25S rDNA信号。这些位点分别位于两条长、两条相对长、两条中、两条相对短的染色体上。这两个5S rDNA位点位于相对较短的染色体的着丝粒位置,不具有18S-5.8S-25S rDNA位点。rDNA位点的数量和位置在幼苗间是稳定的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of ribosomal RNA genes in apple (Malus × domestica) using fluorescence in situ hybridization
The locations of the 18S-5.8S-25S and 5S ribosomal RNA genes (rDNAs) on the chromosomes in the seedlings obtained from open-pollination of apple ‘Sensyu’ (Malus × domestica Borkh.) were determined using fluorescence in situ hybridization (FISH). 18S-5.8S-25S and 5S rDNA probes were labeled with biotin and hybridization signals were detected using a fluorescein isothiocyanate (FITC)-avidin conjugate on the chromosomes counterstained with DAPI. The 18S-5.8S-25S rDNA signals were detected in the telomeric positions of eight chromosomes among 34. These sites were located on two long, two relatively long, two medium, and two relatively short chromosomes. The two 5S rDNA sites were located at centromeric positions of relatively short chromosomes which do not possess 18S-5.8S-25S rDNA sites. The numbers and positions of rDNA sites were stable among the seedlings.
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