Bedo D G
Division of Entomology, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT, Australia.
Genome. 1992 Apr;35(2):283-93. doi: 10.1139/g92-044.
The location of genes coding for 18S and 28S ribosomal RNA in mitotic and polytene cells of Lucilia cuprina and Chrysomya bezziana was investigated using in situ hybridization of an 18 + 28S ribosomal gene probe and silver staining. In both species ribosomal genes were localized to secondary constriction regions in sex chromosome heterochromatin. In L. cuprina mitotic cells the probe hybridizes to a distal secondary constriction region in the short arms of the X and Y chromosomes. In C. bezziana mitotic chromosomes ribosomal genes were located in distal secondary constriction regions in the long arms of the X and Y chromosomes. In polytene trichogen cells of both species, hybridization results varied with the level of polyteny. Cells of low polyteny have a single hybridization site, but with greater polytenization, increasing numbers of extrachromosomal fragments strongly hybridize to the ribosomal gene probe. No hybridization occurs in structures representing the sex chromosomes or in the autosomes. These results indicate that fragmentation and dispersal of the nucleolus occurs during polytenization. Silver staining of both unsquashed and squashed polytene nuclei show identical behaviour of multiple, varied-sized nucleolar bodies, thus confirming the in situ hybridization results. Uridine incorporation studies in L. cuprina indicated that transcription occurs in extrachromosomal bodies similar to nucleolar fragments. Nucleolar fragmentation is more pronounced in L. cuprina males, particularly in those with the translocation T(Y;2)540. Chromosomally normal C. bezziana show nucleolar fragmentation levels similar to that in L. cuprina males. Ribosomal genes are disproportionately replicated in trichogen cells to a much greater extent than surrounding heterochromatin. Nucleolar fragmentation may be a gene amplification system, but it is not known to what degree, relative to diploid amounts, ribosomal genes replicate in trichogen cells.
利用18 + 28S核糖体基因探针原位杂交和银染技术,研究了铜绿蝇和致倦库蚊有丝分裂细胞及多线细胞中编码18S和28S核糖体RNA的基因位置。在这两个物种中,核糖体基因均定位于性染色体异染色质的次缢痕区域。在铜绿蝇有丝分裂细胞中,探针与X和Y染色体短臂的远端次缢痕区域杂交。在致倦库蚊有丝分裂染色体中,核糖体基因位于X和Y染色体长臂的远端次缢痕区域。在这两个物种的多线化毛原细胞中,杂交结果随多线化程度而变化。低多线化细胞有一个单一杂交位点,但随着多线化程度增加,越来越多的染色体外片段强烈杂交至核糖体基因探针。在代表性染色体的结构或常染色体中未发生杂交。这些结果表明,核仁在多线化过程中发生断裂和分散。未压片和压片的多线化细胞核的银染显示,多个大小各异的核仁体表现出相同行为,从而证实了原位杂交结果。铜绿蝇的尿苷掺入研究表明,转录发生在类似于核仁片段的染色体外小体中。核仁断裂在铜绿蝇雄性中更为明显,尤其是那些具有T(Y;2)540易位的个体。染色体正常的致倦库蚊显示出与铜绿蝇雄性相似的核仁断裂水平。核糖体基因在毛原细胞中的复制比例远高于周围的异染色质。核仁断裂可能是一种基因扩增系统,但相对于二倍体数量,核糖体基因在毛原细胞中的复制程度尚不清楚。