...
首页> 外文期刊>Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology >Meiotic pairing and gene expression disturbance in germ cells from an infertile boar with a balanced reciprocal autosome-autosome translocation
【24h】

Meiotic pairing and gene expression disturbance in germ cells from an infertile boar with a balanced reciprocal autosome-autosome translocation

机译:不育公猪生殖细胞减数分裂配对和基因表达紊乱,平衡的常染色体-常染色体易位

获取原文
获取原文并翻译 | 示例
           

摘要

Individuals carrying balanced constitutional reciprocal translocations generally have a normal phenotype, but often present reproductive disorders. The aim of our research was to analyze the meiotic process in an oligoasthenoteratospermic boar carrying an asymmetric reciprocal translocation involving chromosomes 1 and 14. Different multivalent structures (quadrivalent and trivalent plus univalent) were identified during chromosome pairing analysis. Some of these multivalents were characterized by the presence of unpaired autosomal segments with histone gamma H2AX accumulation sometimes associated with the XY body. Gene expression in spermatocytes was studied by RNA-DNA-FISH and microarray-based testis transcriptome analysis. Our results revealed a decrease in gene expression for chromosomes 1 and 14 and an up-regulated expression of X-chromosome genes for the translocated boar compared with normal individuals. We hypothesized that the observed meiotic arrest and reproductive failure in this boar might be due to silencing of crucial autosomal genes (MSUC) and disturbance of meiotic sex chromosome inactivation (MSCI). Further analysis revealed abnormal meiotic recombination (frequency and distribution) and the production of a high rate of unbalanced spermatozoa.
机译:携带平衡的体位易位的个体通常具有正常的表型,但经常表现出生殖障碍。我们的研究目的是分析携带不对称倒易位涉及1号和14号染色体的少动脉粥样硬化精公猪的减数分裂过程。在染色体配对分析中鉴定出不同的多价结构(四价和三价加一价)。这些多价中的一些以不成对的常染色体区段为特征,组氨酸γH2AX积累有时与XY体有关。通过RNA-DNA-FISH和基于微阵列的睾丸转录组分析研究了精细胞中的基因表达。我们的结果显示,与正常个体相比,染色体1和14的基因表达下降,而易位野猪的X染色体基因表达上调。我们假设在该公猪中观察到的减数分裂停滞和生殖衰竭可能是由于关键常染色体基因(MSUC)沉默和减数分裂性染色体失活(MSCI)引起的。进一步的分析显示减数分裂重组异常(频率和分布)以及高比率的不平衡精子产生。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号