Cabrero Josefa, Camacho Juan Pedro M
Departamento de Genética, Facultad de Ciencias, Universidad de Granada, 18071, Granada, Spain.
Chromosome Res. 2008;16(4):595-607. doi: 10.1007/s10577-008-1214-x. Epub 2008 Apr 26.
We investigate regularities and restrictions in chromosome location of ribosomal RNA genes, analysed by fluorescent in situ hybridization (FISH), and their phenotypic expression assessed by nucleolus formation at first meiotic prophase cells, analysed by silver impregnation, in 49 grasshopper species. High variation was found for rDNA location between species within most genera analysed. The mean haploid number of rDNA loci detected by FISH was 2.47, but some species had up to 10 loci. Chromosome distribution of rDNA loci differed between the Gomphocerinae and Oedipodinae subfamilies, most loci being proximal to the centromere in the former and distal to it in the latter. Chromosomes 2, 3 and X frequently carried rDNA in Gomphocerinae species with 2n male symbol=17 chromosomes, whereas chromosomes 6 and 9 were the most frequent rDNA locations in the Oedipodinae. About 13% of the 126 rDNA loci detected by FISH were silent, although this figure might be even higher. The comparison of FISH and silver-impregnation results also suggested the existence of cryptic NORs, i.e. those forming small nucleoli with no apparent presence of rDNA revealed by FISH. This was especially clear after the same cells in two species were sequentially treated with both silver impregnation and FISH. The abundance of silent and cryptic loci might thus suggest that rDNA spreads through grasshopper genomes by the Dubcovsky and Dvorak mechanism-that is, the transposition of a few rRNA genes to new chromosome locations, their amplification giving rise to new NORs, and the elimination of the old NORs. The cryptic NORs might correspond to nascent NORs, i.e. a few rRNA gene copies moved to new locations, whereas the inactive rDNA loci might correspond to those being in the process of elimination.
我们研究了核糖体RNA基因在染色体上的定位规律和限制(通过荧光原位杂交(FISH)进行分析),以及它们的表型表达(通过银染法分析第一次减数分裂前期细胞中的核仁形成来评估),涉及49种蚱蜢。在所分析的大多数属内,物种间的rDNA定位存在高度变异。通过FISH检测到的rDNA位点的单倍体平均数为2.47,但有些物种有多达10个位点。rDNA位点的染色体分布在槌角蝗亚科和斑翅蝗亚科之间有所不同,前者的大多数位点靠近着丝粒,而后者的位点远离着丝粒。在具有2n♂=17条染色体的槌角蝗亚科物种中,2号、3号染色体和X染色体经常携带rDNA,而在斑翅蝗亚科中,6号和9号染色体是最常见的rDNA定位染色体。通过FISH检测到的126个rDNA位点中约有13%是沉默的,尽管这一数字可能更高。FISH和银染结果的比较也表明存在隐性核仁组织区,即那些形成小核仁但FISH未显示明显rDNA存在的区域。在两个物种的相同细胞先后用银染法和FISH处理后,这一点尤为明显。沉默和隐性位点的丰富可能表明rDNA通过杜布科夫斯基和德沃夏克机制在蚱蜢基因组中传播,即少数rRNA基因转座到新的染色体位置,它们的扩增产生新的核仁组织区,同时旧的核仁组织区被消除。隐性核仁组织区可能对应于新生的核仁组织区,即少数rRNA基因拷贝转移到新位置,而无活性的rDNA位点可能对应于正在被消除的那些位点。