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褐软蚧的B染色体:一条利用全基因组减数分裂驱动的自私染色体。

The B Chromosome of Pseudococcus viburni: A Selfish Chromosome that Exploits Whole-Genome Meiotic Drive.

作者信息

Vea Isabelle M, de la Filia Andrés G, Jaron Kamil S, Barlow Scott E J, Herbette Marion, Mongue Andrew J, Nelson Ross, Ruiz-Ruano Francisco J, Ross Laura

机构信息

Department of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, USA.

School of Biological Sciences, Institute of Ecology and Evolution, The University of Edinburgh, Edinburgh EH9 3FL, UK.

出版信息

Genome Biol Evol. 2025 Jan 6;17(1). doi: 10.1093/gbe/evae257.

Abstract

Meiosis is generally a fair process: each chromosome has a 50% chance of being included into each gamete. However, meiosis can become aberrant with some chromosomes having a higher chance of making it into gametes than others. Yet, why and how such systems evolve remains unclear. Here, we study the unusual reproductive genetics of mealybugs, where only maternal-origin chromosomes are included in gametes during male meiosis, while paternal chromosomes are eliminated. One species-Pseudococcus viburni-has a segregating B chromosome that drives by escaping paternal genome elimination. We present whole genome and gene expression data from lines with and without B chromosomes. We identify B-linked sequences including 204 protein-coding genes and a satellite repeat that makes up a significant proportion of the chromosome. The few paralogs between the B and the core genome are distributed throughout the genome, arguing against a simple, or at least recent, chromosomal duplication of one of the autosomes to create the B. We do, however, find one 373 kb region containing 146 genes that appears to be a recent translocation. Finally, we show that while many B-linked genes are expressed during meiosis, most of these are encoded on the recently translocated region. Only a small number of B-exclusive genes are expressed during meiosis. Of these, only one was overexpressed during male meiosis, which is when the drive occurs: an acetyltransferase involved in H3K56Ac, which has a putative role in meiosis and is, therefore, a promising candidate for further studies.

摘要

减数分裂通常是一个公平的过程

每条染色体进入每个配子的概率为50%。然而,减数分裂可能会出现异常,一些染色体进入配子的概率高于其他染色体。然而,这种系统为何以及如何进化仍不清楚。在这里,我们研究了粉蚧不寻常的生殖遗传学,在雄性减数分裂过程中,只有母本来源的染色体被纳入配子,而父本染色体则被消除。一种名为Pseudococcus viburni的物种有一条正在分离的B染色体,它通过逃避父本基因组消除来驱动自身传递。我们展示了有B染色体和无B染色体品系的全基因组和基因表达数据。我们鉴定出了与B染色体相关的序列,包括204个蛋白质编码基因和一个构成该染色体很大比例的卫星重复序列。B染色体和核心基因组之间的少数旁系同源基因分布在整个基因组中,这表明不太可能是由一条常染色体简单地(或者至少不是近期)发生染色体复制而产生了B染色体。然而,我们确实发现了一个包含146个基因的373 kb区域,它似乎是近期发生的易位。最后,我们表明,虽然许多与B染色体相关的基因在减数分裂期间表达,但其中大多数是在最近易位的区域编码的。在减数分裂期间,只有少数B染色体特有的基因表达。其中,只有一个在雄性减数分裂(即驱动发生的时候)期间过表达:一个参与H3K56Ac的乙酰转移酶,它在减数分裂中可能具有一定作用,因此是进一步研究的一个有前景的候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be59/11776215/5ad236ea6a37/evae257f1.jpg

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