差异性基因表达的并行转移揭示了鱼类的融合小型化
Emily M Troyer1,2, William T White3, Ricardo Betancur-R4
1Department of Biology, University of Oklahoma, Norman, OK 73019.
概括
鱼的小型化是由细胞数量的遗传调节驱动的. 微型物种过度表达生长抑制剂,而大体物种高调生长促进剂,揭示了保存的深度时间尺寸控制机制.
科学领域:
- 进化生物学是进化的生物学.
- 基因组学就是基因组学.
- 分子生物学分子生物学
背景情况:
- 身体大小是脊椎动物的一个关键特征,影响生物学,生态学和生理学.
- 微型化,即极度减少身体尺寸,虽然很普遍,但人们对其了解甚少.
- 戈比鱼 (Gobioidei) 是世界上最小的脊椎动物之一,为研究减小尺寸提供了一个模型.
研究的目的:
- 研究鱼体型进化和小型化背后的分子机制.
- 为了确定与Gobioidei分类中的小和大体型重复进化的相关的基因和途径.
主要方法:
- 产生了162个鱼物种的全基因组分类.
- 在微型和大体鱼物种之间进行了比较的转录学.
- 分析了已识别的ortologs的差异性基因表达和功能配置文件.
主要成果:
- 确定了54个微型和大体物种之间差异表达的1对1的ortologs.
- 微型物种过度表达生长抑制剂 (例如CDKN1B,ING2),与细胞增殖减少相关.
- 大型物种可调节增长促进体 (例如TGFB3),与组织发育和信号相关.
结论:
- 细胞数量的调节是脊椎动物体型控制的关键机制.
- 尺寸调节途径的宏观进化趋同已经发生在深层进化时间 (自欧以来).
- 对于理解基本的脊椎动物体型演变来说,研究像戈比这样的非模型生物是至关重要的.
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