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Regularities in simple sequence repeat variations induced by a cross of resynthesized Brassica napus and natural Brassica napus

机译:简单序列的规律重复由重新合成的芸苔和天然芸苔内插口的交叉引起的重复变化

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Interspecific hybridization can induce extensive variation in genome sequences, including simple sequence repeat (SSR) regions. To determine the characteristics of SSR variation induced by interspecific hybridization and the possible effect of SSR variation on gene function, we constructed a Brassica napus doubled-haploid (DH) population from a cross between natural B. napus and resynthesized B. napus (B. oleracea × B. rapa) and identified, located, sequenced and functionally annotated SSR variants. The results showed that novel SSR variants were generated in the F1 generation and maintained in the introgressed DH population. Elimination of sequences carrying SSRs also occurred in the F1 hybrids, with three times as many sequences lost in the introgressed DH population compared to in the F1 hybrids, probably due to non-homologous recombination. The degree of SSR variation observed depended primarily on the number of SSR repeats and secondarily on the nucleotide composition of the SSR motifs. In the introgressed DH population, many genes containing SSRs exhibited frameshift mutations (62.5%) due to the expansion or contraction of the SSR motifs following deletion (25%) or insertion (12.5%) mutations. Most genes harboring SSR variants were associated with vital metabolic processes, such as protein or DNA metabolic processes. The SSR variation induced by interspecific hybridization reflects an intrinsic property of species adaptability post-hybridization through variation. This study is beneficial to understanding the origin of SSRs and the effects of SSR mutation on polyploid genomes.Pages 35-46 |
机译:间隙杂交可以诱导基因组序列的广泛变化,包括简单的序列重复(SSR)区域。为了确定各种杂交诱导的SSR变化的特征和SSR变异对基因功能的可能影响,我们构建了来自天然B. Napus之间的交叉的Brassica Napus双倍倍增(DH)群体,并重新合成B. Napus(B. Oleracea×B.APA)并鉴定,定位,测序和功能注释的SSR变体。结果表明,在F1生成中产生了新的SSR变体并保持在狭窄的DH人口中。消除携带SSRS的序列也发生在F1杂交体中,与在F1杂交体中相比,在狭窄的DH群体中损失的许多序列可能是由于非同源重组的三倍。观察到的SSR变化程度主要取决于SSR重复的数量,并在SSR基序的核苷酸组合物上依赖于SSR的数量。在血液血液群体中,由于SSR基序在缺失(25℃)或插入(12.5℃)突变之后,含有SSRS的许多基因表现出框架突变(62.5±5%)。涉及SSR变体的大多数基因与蛋白质或DNA代谢过程如蛋白质或DNA代谢过程有关。三种杂交诱导的SSR变异反映了通过变异的物种适应性的固有性质。本研究有利于理解SSR的起源和SSR突变对多倍体基因组的影响。35-46 |

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    《Plant Omics》 |2014年第1期|共12页
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