Orooji Fatemeh, Mirzaghaderi Ghader, Kuo Yi-Tzu, Fuchs Jörg
Department of Agronomy and Plant Breeding, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran.
Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Gatersleben, Germany.
Front Plant Sci. 2022 Jun 9;13:917310. doi: 10.3389/fpls.2022.917310. eCollection 2022.
is a small genus belonging to the Ranunculaceae family which is presumably originated and distributed in Aegean and the adjacent Western-Irano-Turanian region. Comparative repeat analysis of , and was performed using low-pass Illumina genomic reads followed by karyotyping and FISH mapping of seven species using the identified repeats and ribosomal DNA (rDNA) probes. High- and moderate-copy repeat sequences occupy 57.52, 59.01, and 64.73% of , and genomes, respectively. Roughly, half of the genomes are retrotransposons (class I transposons), while DNA transposons (class II transposons) contributed to only about 2% of the genomes. The analyzed species possess large genomes of about 7.4 to 12.4 Gbp/1C. Only two satellite repeats in , one in and four in were identified, which were mostly (peri)centromeric and represented about 1% of each genome. A high variation in number and position of 45S rDNA loci were found among species. Interestingly, in , each chromosome revealed at least one 45S rDNA site and one of them occurs in hemizygous condition. Based on the chromosome numbers, genome size and (peri)centromeric satellites, three karyotype groups were observed: Two with 2 = 2 = 12 and a karyotype formula of 10m + 2t (including , , as the first group and and as the second group) and a more distant group with 2 = 2 = 14 and a karyotype formula of 8m + 2st + 4t (including and ). These karyotype groups agreed with the phylogenetic analysis using ITS and L sequences. We conclude that variation in (peri)centromeric sequences, number and localization of rDNA sites as well as chromosome number (dysploidy) are involved in the diversification of the genus .
是毛茛科的一个小属,大概起源于爱琴海及相邻的西伊朗 - 图兰地区并分布于此。利用低深度Illumina基因组 reads 对[物种名称未给出]、[物种名称未给出]和[物种名称未给出]进行了比较重复序列分析,随后使用鉴定出的重复序列和核糖体DNA(rDNA)探针,对7种[物种名称未给出]进行了核型分析和荧光原位杂交(FISH)定位。高拷贝和中拷贝重复序列分别占[物种名称未给出]、[物种名称未给出]和[物种名称未给出]基因组的57.52%、59.01%和64.73%。大致来说,基因组的一半是逆转座子(I类转座子),而DNA转座子(II类转座子)仅占基因组的约2%。所分析的[物种名称未给出]物种拥有大约7.4至12.4 Gbp/1C的大基因组。在[物种名称未给出]中仅鉴定出两个卫星重复序列,在[物种名称未给出]中有一个,在[物种名称未给出]中有四个,它们大多位于(近)着丝粒区域,约占每个基因组的1%。在[物种名称未给出]物种中发现45S rDNA位点的数量和位置存在高度变异。有趣的是,在[物种名称未给出]中,每条染色体至少有一个45S rDNA位点,其中一个以半合子状态出现。基于染色体数目、基因组大小和(近)着丝粒卫星序列,观察到三个核型组:两组2n = 2x = 12,核型公式为10m + 2t(第一组包括[物种名称未给出]、[物种名称未给出]、[物种名称未给出],第二组包括[物种名称未给出]和[物种名称未给出]),以及一个较远的组2n = 2x = 14,核型公式为8m + 2st + 4t(包括[物种名称未给出]和[物种名称未给出])。这些核型组与使用ITS和L序列进行的系统发育分析结果一致。我们得出结论,(近)着丝粒序列的变异、rDNA位点的数量和定位以及染色体数目(整倍体变异)参与了[属名未给出]属的多样化过程。