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利用重复DNA探针和荧光原位杂交技术对蜜蜂(西方蜜蜂)染色体进行表征。

Characterization of honeybee (Apis mellifera L.) chromosomes using repetitive DNA probes and fluorescence in situ hybridization.

作者信息

Beye M, Moritz R F

机构信息

Institut für Biologie, Technische Universität Berlin, Germany.

出版信息

J Hered. 1995 Mar-Apr;86(2):145-50. doi: 10.1093/oxfordjournals.jhered.a111545.

Abstract

Two different repetitive DNA probes of Apis mellifera and ribosomal DNA from Drosophila melanogaster were used to characterize the chromosomal set of the honeybee (n = 16). The probes were hybridized to chromosome preparations of haploid testis tissue from drone larvae using fluorescence in situ hybridization (FISH). The honeybee probes hybridized to the telomeric (Alu I family) and centromeric region (Ava I family) of most chromosomes. The rDNA probe labeled two chromosomes only. Combination of the three probes yielded labeled patterns allowing us to identify each chromosome of the honeybee individually. This is the first report of an unambiguous identification of the chromosomal set of the honeybee, since classical banding techniques failed to yield clear patterns for identification. The consensus sequence of the centromeric reiterated probe (Ava I family) has a length of about 550 nucleotides and shows no homology to other known sequences. However, the structural organization of a 130-nucleotides long motif forming the unusually homogeneous 550 nucleotides repeat is similar to those found in mammals' repetitive DNAs.

摘要

使用来自意大利蜜蜂的两种不同重复DNA探针和来自黑腹果蝇的核糖体DNA来表征蜜蜂(n = 16)的染色体组。利用荧光原位杂交(FISH)技术,将这些探针与雄蜂幼虫单倍体睾丸组织的染色体标本进行杂交。蜜蜂探针与大多数染色体的端粒(Alu I家族)和着丝粒区域(Ava I家族)杂交。核糖体DNA探针仅标记了两条染色体。三种探针的组合产生了可使我们单独识别蜜蜂每条染色体的标记模式。这是关于明确鉴定蜜蜂染色体组的首次报道,因为传统的显带技术未能产生清晰的识别模式。着丝粒重复探针(Ava I家族)的共有序列长度约为550个核苷酸,与其他已知序列无同源性。然而,形成异常均匀的550个核苷酸重复序列的130个核苷酸长基序的结构组织与在哺乳动物重复DNA中发现的结构组织相似。

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