Male-biased recombination at chromosome ends in a songbird revealed by precisely mapping crossover positions.

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY
Hongkai Zhang, Max Lundberg, Suvi Ponnikas, Dennis Hasselquist, Bengt Hansson
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Abstract

Recombination plays a crucial role in evolution by generating novel haplotypes and disrupting linkage between genes, thereby enhancing the efficiency of selection. Here, we analyze the genomes of 12 great reed warblers (Acrocephalus arundinaceus) in a 3-generation pedigree to identify precise crossover positions along the chromosomes. We located more than 200 crossovers and found that these were highly concentrated toward the telomeric ends of the chromosomes. Apart from this major pattern in the recombination landscape, we found significantly higher frequencies of crossovers in genic compared with intergenic regions, and in exons compared with introns. Moreover, while the number of recombination events was similar between the sexes, the crossovers were located significantly closer to the ends of paternal compared with maternal chromosomes. In conclusion, our study of the great reed warbler revealed substantial variation in crossover frequencies within chromosomes, with a distinct bias toward the sub-telomeric regions, particularly on the paternal side. These findings emphasize the importance of thoroughly screening the entire length of chromosomes to characterize the recombination landscape and uncover potential sex-biases in recombination.

通过精确绘制交叉位置图揭示鸣禽染色体末端的雄性偏向重组。
重组通过产生新的单倍型和破坏基因之间的联系,从而提高选择的效率,在进化过程中发挥着至关重要的作用。在这里,我们分析了三代血统中十二只大苇莺(Acrocephalus arundinaceus)的基因组,以确定染色体上的精确交叉位置。我们找到了 200 多个交叉点,发现这些交叉点高度集中在染色体的端粒末端。除了这一主要的重组模式外,我们还发现基因区的交叉频率明显高于基因间区,外显子的交叉频率明显高于内含子。此外,虽然两性之间重组事件的数量相似,但交叉的位置明显更靠近父系染色体的末端,而不是母系染色体的末端。总之,我们对大苇莺的研究揭示了染色体内交叉频率的巨大差异,而且明显偏向于亚组群区域,尤其是父系。这些发现强调了彻底筛查整个染色体长度的重要性,以确定重组情况的特征并发现重组中潜在的性别偏倚。
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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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