Hirai H, Yamamoto M T, Ogura K, Satta Y, Yamada M, Taylor R W, Imai H T
Primate Research Institute, Kyoto University, Aichi-ken, Japan.
Chromosoma. 1994 Jun;103(3):171-8. doi: 10.1007/BF00368009.
Chromosomal localization of rDNA in samples of five taxa of the Mymecia pilosula species complex (Hymenoptera: Formicidae: Myrmeciinae) with 2n = 3 (M. croslandi), 8 (M. imaii), 10 (M. banksi), 18 (M. haskinsorum), and 27 (M. pilosula) was carried out by fluorescence in situ hybridization (FISH) using cloned M. croslandi rDNA (pMc.r2) including the coding region for 28S rRNA. Results show that (1) the 28S rDNA in the genome of these ants is repetitive and is localized in pericentromeric C-bands, (2) the number of chromosomes carrying rDNA is two in M. croslandi, M. imaii and M. banksi, six in M. haskinsorum and ten in M. pilosula, and (3) only one or two clusters of rRNA genes generate nucleoli in each species. We suggest that the rDNA in the ancestral stock of the M. pilosula complex was localized originally in a pericentromeric C-band, and multiplied by chance with time during saltatory increases in C-banding following episodes of centric fission. Most rDNA multiplied on various chromosomes seems to be inactivated and eliminated from the genome, together with C-bands, by AM-inversion or centric fusion, with the remnant rDNAs dispersed in the genome by centric fission and AM-inversion.
利用包含28S rRNA编码区的克隆克罗斯兰毛蚁rDNA(pMc.r2),通过荧光原位杂交(FISH)对毛蚁属物种复合体五个分类单元(膜翅目:蚁科:毛蚁亚科)的样本进行rDNA的染色体定位,这五个分类单元的染色体数目分别为2n = 3(克罗斯兰毛蚁)、8(今泉毛蚁)、10(班克斯毛蚁)、18(哈斯金斯毛蚁)和27(毛蚁)。结果表明:(1)这些蚂蚁基因组中的28S rDNA具有重复性,且定位于着丝粒周围的C带;(2)携带rDNA的染色体数量在克罗斯兰毛蚁、今泉毛蚁和班克斯毛蚁中为两条,在哈斯金斯毛蚁中为六条,在毛蚁中为十条;(3)每个物种中只有一或两个rRNA基因簇形成核仁。我们认为,毛蚁属物种复合体原始种群中的rDNA最初定位于着丝粒周围的C带,在着丝粒分裂后的C带跳跃式增加过程中,随时间偶然倍增。多数在不同染色体上倍增的rDNA似乎通过AM倒位或着丝粒融合与C带一起被基因组灭活并消除,残余的rDNA通过着丝粒分裂和AM倒位分散于基因组中。