Cabrero Josefa, López-León Ma Dolores, Teruel María, Camacho Juan Pedro M
Departamento de Genética, Universidad de Granada, 18071, Granada, Spain.
Chromosome Res. 2009;17(3):397-404. doi: 10.1007/s10577-009-9030-5. Epub 2009 Apr 1.
We analyse chromosome location of H3 and H4 histone gene clusters by fluorescence in-situ hybridization (FISH) in 35 species of Acrididae grasshoppers belonging to seven subfamilies. As in other organisms, H3 and H4 co-localized in the same chromosome region in the 11 species where double FISH was performed with the H3 and H4 DNA probes. Chromosome location of H3-H4 histone gene clusters showed high regularity in the species analysed, with all of them carrying a single H3-H4 cluster in an autosome which, in most cases, was located interstitially in the proximal chromosome third. In 17 out of the 21 species with 2n masculine = 23 acrocentric chromosomes, the H3-H4-carrying autosome was about eighth in order of decreasing size. Two of the four exceptions changed H3-H4 localization to proximal (Pezotettix giornae) or distal (Tropidopola graeca) in the eighth-sized autosome, but the remainder (the two Eyprepocnemis species) showed the H3-H4 cluster distally located in the second-sized autosome. All 14 species with 2n masculine = 17 chromosomes (including three long metacentric autosome pairs, five acrocentric autosome pairs and an acrocentric X chromosome) carried an interstitial H3-H4 cluster in the short arm of the smallest of the three long metacentric pairs. These results suggest that chromosome location of H3-H4 histone gene clusters seem to be highly conservative in Acrididae grasshoppers. The change in H3-H4 location from the acrocentric medium-sized autosome in the 2n masculine = 23 karyotype to the long metacentric autosome in the 2n masculine = 17 karyotype is most parsimoniously explained by common ancestry, i.e. by the involvement of the H3-H4-carrying acrocentric in the centric fusion that gave rise to the smallest of the three long metacentric autosomes of 2n masculine = 17 species.
我们通过荧光原位杂交(FISH)分析了隶属于七个亚科的35种蝗科蝗虫中H3和H4组蛋白基因簇的染色体定位。与其他生物一样,在用H3和H4 DNA探针进行双重FISH的11个物种中,H3和H4共定位于同一染色体区域。在所分析的物种中,H3 - H4组蛋白基因簇的染色体定位显示出高度的规律性,所有物种在一条常染色体上都携带一个单一的H3 - H4簇,在大多数情况下,该簇位于近端染色体三分之一的间质位置。在2n雄性 = 23条近端着丝粒染色体的21个物种中的17个物种中,携带H3 - H4的常染色体按大小递减顺序约为第八大。四个例外中的两个将H3 - H4定位改变为第八大常染色体上的近端(乔氏佩佐蝗)或远端(希腊热带蝗),但其余的(两个艾氏蝗属物种)显示H3 - H4簇位于第二大常染色体的远端。所有2n雄性 = 17条染色体的14个物种(包括三对长的中着丝粒常染色体、五对着丝粒常染色体和一条近端着丝粒X染色体)在三对长的中着丝粒对中最小的一条的短臂上携带一个间质H3 - H4簇。这些结果表明,H3 - H4组蛋白基因簇的染色体定位在蝗科蝗虫中似乎高度保守。H3 - H4定位从2n雄性 = 23核型的近端着丝粒中型常染色体变为2n雄性 = 17核型的长中着丝粒常染色体,最简约的解释是共同祖先,即携带H3 - H4的近端着丝粒参与了导致2n雄性 = 17物种的三对长中着丝粒常染色体中最小的一条的着丝粒融合。