Qin QinBo, Liu QiWen, Wang ChongQing, Cao Liu, Zhou YuWei, Qin Huan, Zhao Chun, Liu ShaoJun
State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Sciences, Hunan Normal University, Changsha, China.
Front Genet. 2019 May 15;10:437. doi: 10.3389/fgene.2019.00437. eCollection 2019.
The autotetraploid fish (4 = 200, RRRR) (abbreviated as 4RR) resulted from the whole genome duplication of red crucian carp ( red var., 2 = 100, RR) (abbreviated as RCC). During investigation of the influence of polyploidization on organization and evolution of the multigene family of rDNA, molecular organization and chromosomal localization of the rDNA were characterized in autotetraploid fish. By sequence analysis of the coding region () and adjacent non-transcribed spacer (NTS), three distinct rDNA units (type I: 203 bp; type II: 340 bp; and type III: 477bp) were identified and characterized in 4RR. These rDNA units were inherited from their female parent (RCC), in which obvious base variations in NTS and array recombination of repeat units were found. Using fluorescence hybridization employing different rDNA units as probes, these rDNA clusters were localized in chromosomes of 4RR, respectively, and showed obvious loss of chromosomal loci (type I and type II). Our data revealed genetic variation of the rDNA multigene family in the genome of autopolyploid fish. Furthermore, results provided new insights into the evolutionary patterns of this vertebrate multigene family.
同源四倍体鱼(4n = 200,RRRR)(简称为4RR)由红鲫(红变种,2n = 100,RR)(简称为RCC)的全基因组加倍产生。在研究多倍体化对rDNA多基因家族的组织和进化的影响时,对同源四倍体鱼的rDNA的分子组织和染色体定位进行了表征。通过对编码区()和相邻非转录间隔区(NTS)的序列分析,在4RR中鉴定并表征了三个不同的rDNA单元(I型:203 bp;II型:340 bp;III型:477 bp)。这些rDNA单元遗传自其母本(RCC),在其中发现了NTS中明显的碱基变异和重复单元的阵列重组。使用不同的rDNA单元作为探针进行荧光原位杂交,这些rDNA簇分别定位在4RR的染色体上,并显示出明显的染色体位点缺失(I型和II型)。我们的数据揭示了同源多倍体鱼基因组中rDNA多基因家族的遗传变异。此外,结果为该脊椎动物多基因家族的进化模式提供了新的见解。