Danilova Tatiana V, Friebe Bernd, Gill Bikram S, Poland Jesse, Jackson Eric
Wheat Genetics Resource Center, Department of Plant Pathology, Throckmorton Plant Sciences Center, Kansas State University, Manhattan, KS, USA.
Cytogenet Genome Res. 2018;154(1):45-55. doi: 10.1159/000487183. Epub 2018 Feb 28.
Interspecific or introgressive hybridization is one of the driving forces in plant speciation, producing allopolyploids or diploids with rearranged genomes. The process of karyotype reshaping following homoploid interspecific hybridization has not been studied experimentally. Interspecific hybridization is widely used in plant breeding to increase genetic diversity and introgress new traits. Numerous introgression stocks were developed for hexaploid wheat Triticum aestivum L. (2n = 6x = 42, genome AABBDD). Double monosomic lines, containing one alien chromosome from the tertiary gene pool of wheat and one homoeologous wheat chromosome, represent a simplified model for studying chromosome rearrangements caused by interspecific hybridization. The pairing of a chromosome from the tertiary gene pool with a wheat homoeologue is restricted by the activity of the wheat Ph1 gene, thus, rearrangements caused by chromosome breakage followed by the fusion of the broken arms can be expected. We analyzed chromosome aberrations in 4 sets of lines that originated from double monosomics of barley (Hordeum vulgare L.) chromosome 7H and wheat group-7 chromosomes with dicentric or ring chromosomes. The dynamics of wheat-barley dicentric chromosomes during plant development was followed and an increased diversity of rearrangements was observed. Besides the targeted group-7 chromosomes, other wheat chromosomes were involved in rearrangements, as chromosomes broken in the centromeric region fused with other broken chromosomes. In some cells, multi-centric chromosomes were observed. The structure and dosage of the introgressed barley chromatin was changed. The transmission of the rearrangements to the progenies was analyzed. The observed aberrations emphasize the importance of cytogenetic screening in gene introgression projects.
种间杂交或渐渗杂交是植物物种形成的驱动力之一,可产生具有重排基因组的异源多倍体或二倍体。同倍体种间杂交后核型重塑的过程尚未进行实验研究。种间杂交在植物育种中被广泛用于增加遗传多样性和导入新性状。为六倍体小麦普通小麦(2n = 6x = 42,基因组AABBDD)培育了许多渐渗系。双单体品系包含一条来自小麦三级基因库的外源染色体和一条小麦同源染色体,是研究种间杂交引起的染色体重排的简化模型。来自三级基因库的染色体与小麦同源染色体的配对受到小麦Ph1基因活性的限制,因此,可以预期由染色体断裂后断臂融合引起的重排。我们分析了4组品系中的染色体畸变,这些品系源自大麦(Hordeum vulgare L.)7H染色体和小麦7组染色体的双单体,带有双着丝粒或环状染色体。追踪了小麦 - 大麦双着丝粒染色体在植物发育过程中的动态变化,并观察到重排的多样性增加。除了目标7组染色体外,其他小麦染色体也参与了重排,因为在着丝粒区域断裂的染色体与其他断裂染色体融合。在一些细胞中观察到了多着丝粒染色体。渐渗大麦染色质的结构和剂量发生了变化。分析了重排向后代的传递情况。观察到的畸变强调了细胞遗传学筛选在基因渐渗项目中的重要性。