Trapitz P, Glätzer K H, Bünemann H
Institut für Genetik, Heinrich-Heine-Universität Düsseldorf, FRG.
Mol Gen Genet. 1992 Nov;235(2-3):221-34. doi: 10.1007/BF00279364.
The understanding of structure and function of the so-called fertility genes of Drosophila is very limited due to their unusual size--several megabases--and their location on the heterochromatic Y chromosome. Since mapping of these genes has mainly been done by classical cytogenetic analyses using a small number of cytologically visible lampbrush loops as the sole markers for particular fertility genes, the resolution of the genetic map of the Y chromosome is restricted to 3-5 Mb. Here we demonstrate that a substantially finer subdivision of the megabase-sized fertility genes in the subtelomeric regions of the Y chromosome of Drosophila hydei can be achieved by a combination of digestion with restriction enzymes having 6 bp recognition sequences, and pulsed field gel electrophoresis. The physical subdivision is based upon large conserved fragments of repetitive DNA in the size range from 50 up to 1600 kb and refers to the long-range organization of several families of repetitive DNA involved in Y chromosomal transcription processes in primary spermatocytes. We conclude from our results that at least five different families of repetitive DNA specifically transcribed on the lampbrush loops nooses and threads are organized as extended clusters of several hundred kb, essentially free of interspersed non-repetitive sequences.
由于果蝇所谓的育性基因具有不寻常的大小(几个兆碱基)且位于异染色质Y染色体上,对其结构和功能的了解非常有限。由于这些基因的定位主要是通过经典细胞遗传学分析完成的,使用少数细胞学上可见的灯刷环作为特定育性基因的唯一标记,Y染色体遗传图谱的分辨率限制在3 - 5兆碱基。在这里,我们证明通过结合使用具有6碱基识别序列的限制性内切酶消化和脉冲场凝胶电泳,可以实现对海德氏果蝇Y染色体亚端粒区域中兆碱基大小的育性基因进行更精细的细分。物理细分基于大小范围从50到1600千碱基的重复DNA的大保守片段,并且涉及初级精母细胞中参与Y染色体转录过程的几个重复DNA家族的长程组织。我们从结果中得出结论,至少五个不同的重复DNA家族在灯刷环的套索和细丝上特异性转录,它们被组织成几百千碱基的延伸簇,基本上没有散布的非重复序列。