Lakhotia S C, Mishra A
Chromosoma. 1980;81(1):137-50. doi: 10.1007/BF00292428.
A comparative study of fluorescence patterns of heterochromatin in mitotic and polytene chromosomes of seven species belonging to 3 subgroups (melanogaster sub-group: D. melanogaster and D. simulans; montium sub-group: D. kikkawai and D. jambulina; ananassae sub-group: D. ananassae. D. malerkotliana and D. bipectinata) of the melanogaster species group of Drosophila (Sophophora) has been made. Hoechst 33258 (H) fluorescence patterns of mitotic chromosomes reveal differences correlated to the taxonomic groupings of these species. The melanogaster sub-group species have H-bright regions on heterochromatin of all chromosomes; the montium subgroup species have H-bright regions mainly on the 4th and Y-chromosomes; in the ananassae sub-group, while D. ananassae chromosomes do not show any H-bright regions. D. malerkotliana and D. bipectinata have small H-bright segments only on their 4th chromosomes. The H- and quinacrine mustard (QM) fluorescence patterns of larval salivary gland polytene chromocentre in these species, however, do not show the same taxonomic correlation. While D. ananassae and D. kikkawai polytene nuclei lack any H- or QM-bright region in the chromocentre, the remaining species have prominent H- and/or QM-bright region(s). In D. jambulina, the QM-bright regions are generally bigger than H-bright regions, while in D. malerkotliana and D. bipectinata the situation is reversed. Actinomycin D counterstaining prior to H-staining of polytene preparations of each species confirms that the H-bright region/s in the chromocentre are composed of A-T rich sequences. In vivo labelling of salivary gland polytene nuclei with 5-bromo-deoxyuridine for 24 to 48 h and subsequent H-staining reveals that in all the species, the H-bright regions do not replicate in 3rd instar stage and presumably represent the non-replicating alpha heterochromatin. Significantly, in all the species (excepting D. kikkawai and D. ananassae), the size, location and the number of H- and/or QM-bright regions were seen to vary in different polytene nuclei in the same gland. It seems that the organization and the extent of under-replication of alpha heterochromatin varies in different polytene nuclei. Present studies also show that even closely related species differ in the content and organization of H-bright heterochromatin. The 81F band at the base of 3R in D. melanogaster, but not in D. simulans, appears to contain non-replicating H-bright sequences in addition to replicating chromatin.
对果蝇(Sophophora)黑腹果蝇物种组3个亚组(黑腹亚组:黑腹果蝇和拟暗果蝇;山地亚组:喜久井果蝇和贾布林纳果蝇;阿纳萨亚亚组:阿纳萨亚果蝇、马勒科特利亚纳果蝇和双栉果蝇)中7个物种有丝分裂染色体和多线染色体上异染色质的荧光模式进行了比较研究。有丝分裂染色体的Hoechst 33258(H)荧光模式显示出与这些物种分类分组相关的差异。黑腹亚组物种在所有染色体的异染色质上有H亮区;山地亚组物种主要在第4号和Y染色体上有H亮区;在阿纳萨亚亚组中,阿纳萨亚果蝇染色体没有任何H亮区,马勒科特利亚纳果蝇和双栉果蝇仅在其第4号染色体上有小的H亮区片段。然而,这些物种幼虫唾液腺多线染色体中心的H和喹吖因芥子(QM)荧光模式并没有显示出相同的分类相关性。阿纳萨亚果蝇和喜久井果蝇的多线细胞核在染色体中心没有任何H或QM亮区,其余物种有明显的H和/或QM亮区。在贾布林纳果蝇中,QM亮区通常比H亮区大,而在马勒科特利亚纳果蝇和双栉果蝇中情况则相反。对每个物种的多线体制备物进行H染色之前用放线菌素D复染证实,染色体中心的H亮区由富含A - T的序列组成。用5 - 溴脱氧尿苷对唾液腺多线细胞核进行24至48小时的体内标记,随后进行H染色显示,在所有物种中,H亮区在三龄期不复制,大概代表非复制性α异染色质。值得注意的是,在所有物种(除喜久井果蝇和阿纳萨亚果蝇外)中,同一腺体中不同多线细胞核内H和/或QM亮区的大小、位置和数量各不相同。似乎α异染色质的组织和复制不足程度在不同的多线细胞核中有所不同。目前的研究还表明,即使是亲缘关系密切的物种,其H亮异染色质的含量和组织也存在差异。黑腹果蝇3R基部的81F带,而不是拟暗果蝇的,除了复制染色质外,似乎还包含非复制性H亮序列。