The role of meiosis on the evolution of the sex chromosomes

减数分裂对性染色体进化的作用

• 批准号: 8148813
• 负责人: Rafael Camerini-Otero
• 金额: $ 9.56万
• 依托单位: NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8148813
• 关键词: Evolution; Meiosis; Role; Sex Chromosomes

Understanding the evolutionary selective forces that fashioned the sex chromosomes from a putative ancestral autosome pair is a major problem in biology (reviewed in Khil and Camerini-Otero (2005) Crit. Rev. Biochem. Mol. Biol. 40, 313). A few years ago it was reported that genome-wide analyses of C. elegans and D. melanogaster revealed that male-specific genes are underrepresented on the X-chromosome whereas the opposite was reported for about 2 dozen mouse spermatogonial genes. Is the mouse really different? Our analysis of the Spo11 adult mice microarray data provided a time line for the expression of testis genes. We found that those genes expressed in cells late in meiosis, including the majority of testis-enriched genes, are underrepresented on the X. However, early genes are overrepresented. Since the previously published mouse data pertained to early spermatogonial genes only, these results reconcile all the data. Furthermore, we added a missing piece of the puzzle by proposing that the demasculinization (removal of male genes) of the X chromosome in most organisms is influenced by inactivation of the sex chromosomes during male meiosis (see commentary in Reinke (2004) Nat. Genet. 6, 548). One manner by which this reshaping of the X chromosome is achieved is by retrotransposition from the X chromosome to autosomes much more frequently than between autosomes (Shiao et al., in press). Presently, we are not actively working on this project bu plan to start within the next year to investigate how chromosome pairing regulates chromosome silencing.

理解从推定的祖先常染色体对形成性染色体的进化选择力是生物学中的主要问题（综述于Khil和Camerini-Obern（2005）Crit. Rev. Biochem. Mol. 40，313）。几年前，有报道称，对C。elegans和D. melanogaster的研究表明，雄性特异性基因在X染色体上的表达不足，而大约20多个小鼠精原细胞基因的报道正好相反。 老鼠真的不同吗？我们对Spo 11成年小鼠微阵列数据的分析提供了睾丸基因表达的时间线。我们发现那些在减数分裂后期细胞中表达的基因，包括大多数睾丸富集基因，在X染色体上表达不足。 然而，早期基因被过度代表。由于先前发表的小鼠数据仅涉及早期精原细胞基因，因此这些结果与所有数据一致。此外，我们通过提出大多数生物体中X染色体的去雄性化（雄性基因的去除）受到雄性减数分裂期间性染色体失活的影响（参见Reinke（2004）Nat. Genet. 6，548）。 实现X染色体的这种重塑的一种方式是通过从X染色体到常染色体的反转录转座，其频率远高于常染色体之间的转座（Shiao et al.，印刷中）。目前，我们还没有积极开展这个项目，但计划在明年开始研究染色体配对如何调节染色体沉默。