Meiotic segregation and post-meiotic drive of the Festuca pratensis B chromosome.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Chromosome Research Pub Date : 2023-09-02 DOI:10.1007/s10577-023-09728-6
Rahman Ebrahimzadegan, Jörg Fuchs, Jianyong Chen, Veit Schubert, Armin Meister, Andreas Houben, Ghader Mirzaghaderi
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Abstract

In many species, the transmission of B chromosomes (Bs) does not follow the Mendelian laws of equal segregation and independent assortment. This deviation results in transmission rates of Bs higher than 0.5, a process known as "chromosome drive". Here, we studied the behavior of the 103 Mbp-large B chromosome of Festuca pratensis during all meiotic and mitotic stages of microsporogenesis. Mostly, the B chromosome of F. pratensis segregates during meiosis like standard A chromosomes (As). In some cases, the B passes through meiosis in a non-Mendelian segregation leading to their accumulation already in meiosis. However, a true drive of the B happens during the first pollen mitosis, by which the B preferentially migrates to the generative nucleus. During second pollen mitosis, B divides equally between the two sperms. Despite some differences in the frequency of drive between individuals with different numbers of Bs, at least 82% of drive was observed. Flow cytometry-based quantification of B-containing sperm nuclei agrees with the FISH data.

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高羊茅B染色体的减数分裂和减数分裂后驱动。
在许多物种中,B染色体(Bs)的传播不遵循孟德尔的平等分离和独立分类定律。这种偏差导致Bs的传播率高于0.5,这一过程被称为“染色体驱动”。在这里,我们研究了高羊茅103Mbp大B染色体在小孢子发生的所有减数分裂和有丝分裂阶段的行为。大多数情况下,pratensis的B染色体在减数分裂过程中像标准的A染色体(As)一样分离。在某些情况下,B以非孟德尔分离的方式通过减数分裂,导致它们已经在减数分裂中积累。然而,B的真正驱动作用发生在第一次花粉有丝分裂期间,通过这种有丝分裂,B优先迁移到生殖细胞核。在第二次花粉有丝分裂过程中,B在两个精子之间平分。尽管具有不同B数的个体之间的驱动频率存在一些差异,但至少观察到82%的驱动。基于流式细胞术的含B精子细胞核定量与FISH数据一致。
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来源期刊
Chromosome Research
Chromosome Research 生物-生化与分子生物学
CiteScore
4.70
自引率
3.80%
发文量
31
审稿时长
1 months
期刊介绍: Chromosome Research publishes manuscripts from work based on all organisms and encourages submissions in the following areas including, but not limited, to: · Chromosomes and their linkage to diseases; · Chromosome organization within the nucleus; · Chromatin biology (transcription, non-coding RNA, etc); · Chromosome structure, function and mechanics; · Chromosome and DNA repair; · Epigenetic chromosomal functions (centromeres, telomeres, replication, imprinting, dosage compensation, sex determination, chromosome remodeling); · Architectural/epigenomic organization of the genome; · Functional annotation of the genome; · Functional and comparative genomics in plants and animals; · Karyology studies that help resolve difficult taxonomic problems or that provide clues to fundamental mechanisms of genome and karyotype evolution in plants and animals; · Mitosis and Meiosis; · Cancer cytogenomics.
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