Transcriptomic Architecture of Reproductive Plasticity

S. Renn, N. Aubin‐Horth
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引用次数: 1

Abstract

Several species show diversity in reproductive patterns that result from phenotypic plasticity. This reproductive plasticity is found for example in mate choice, parental care, reproduction suppression, reproductive tactics, sex role, and sex reversal. Studying the genome-wide changes in transcription that are associated with these plastic phenotypes will help answer several questions, including those regarding which genes are expressed and where they are expressed when an individual is faced with a reproductive choice, as well as those regarding whether males and females have the same brain genomic signature when they express the same behaviors, or if they activate sex-specific molecular pathways to output similar behavioral responses. The comparative approach of studying transcription in a wide array of species allows us to uncover genes, pathways, and biological functions that are repeatedly co-opted (“genetic toolkit”) as well as those that are unique to a particular system (“genomic signature”). Additionally, by quantifying the transcriptome, a labile trait, using time series has the potential to uncover the causes and consequences of expressing one plastic phenotype or another. There are of course gaps in our knowledge of reproductive plasticity, but no shortage of possibilities for future directions.
生殖可塑性的转录组结构
由于表型可塑性,一些物种表现出生殖模式的多样性。这种生殖可塑性可以在配偶选择、亲代抚育、繁殖抑制、繁殖策略、性别角色和性别逆转等方面找到。研究与这些可塑性表型相关的全基因组转录变化将有助于回答几个问题,包括当个体面临生殖选择时,哪些基因被表达以及在哪里表达,以及当男性和女性表达相同的行为时,他们是否具有相同的大脑基因组特征,或者他们是否激活了性别特异性分子途径以输出相似的行为反应。研究多种物种转录的比较方法使我们能够发现反复选择的基因、途径和生物功能(“遗传工具包”)以及特定系统特有的基因、途径和生物功能(“基因组特征”)。此外,通过量化转录组(一种不稳定的性状),使用时间序列有可能揭示表达一种或另一种塑性表型的原因和后果。当然,我们对生殖可塑性的认识还存在差距,但未来的发展方向并不缺乏可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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