Wang Daryi, Sung Huang-Mo, Wang Tzi-Yuan, Huang Chih-Jen, Yang Peggy, Chang Tiffany, Wang Yang-Chao, Tseng Da-Lun, Wu Jen-Pey, Lee Tso-Ching, Shih Ming-Che, Li Wen-Hsiung
Research Center for Biodiversity, Academia Sinica, Taipei, Taiwan.
Genome Res. 2007 Aug;17(8):1161-9. doi: 10.1101/gr.6328907. Epub 2007 Jul 5.
Both cis- and trans-regulatory mutations contribute to gene expression divergence within and between species. To estimate their relative contributions, we examined two yeast strains, BY (a laboratory strain) and RM (a wild strain), for their gene-expression divergence by microarray. Using these data and published ChIP-chip data, we obtained a set of single-regulator-regulated genes that showed expression divergence between BY and RM. We randomly selected 50 of these genes for further study. We developed a step-by-step approach to assess the relative contributions of cis- and trans-variations to expression divergence by using pyrosequencing to quantify the mRNA levels of the BY and RM alleles in the same culture (co-culture) and in hybrid diploids. Forty genes showed expression divergence between the two strains in co-culture, and pyrosequencing of the BY/RM hybrid diploids showed that 45% (18/40) can be attributed to differences in trans-acting factors alone, 17.5% (7/40) mainly to trans-variations, 20% (8/40) to both cis- and trans-acting factors, 7.5% (3/40) mainly to cis-variations, and 10% (4/40) to cis-acting factors alone. In addition, we replaced the BY promoter by the RM promoter in each of 10 BY genes that were found from our microarray data to have expression divergence between BY and RM, and in each case our quantitative PCR analysis revealed a cis effect of the promoter replacement on gene expression. In summary, our study suggests that trans-acting factors play the major role in expression evolution between yeast strains, but the role of cis variation is also important.
顺式和反式调控突变都对物种内部和物种之间的基因表达差异有贡献。为了估计它们的相对贡献,我们通过微阵列研究了两种酵母菌株,BY(一种实验室菌株)和RM(一种野生菌株)的基因表达差异。利用这些数据和已发表的染色质免疫沉淀芯片(ChIP-chip)数据,我们获得了一组在BY和RM之间表现出表达差异的单调控因子调控基因。我们随机选择了其中50个基因进行进一步研究。我们开发了一种逐步的方法,通过焦磷酸测序来量化同一培养物(共培养)和杂交二倍体中BY和RM等位基因的mRNA水平,以评估顺式和反式变异对表达差异的相对贡献。在共培养中,40个基因在两种菌株之间表现出表达差异,对BY/RM杂交二倍体的焦磷酸测序表明,45%(18/40)可仅归因于反式作用因子的差异,17.5%(7/40)主要归因于反式变异,20%(8/40)归因于顺式和反式作用因子,7.5%(3/40)主要归因于顺式变异,10%(4/40)仅归因于顺式作用因子。此外,我们用RM启动子替换了从我们的微阵列数据中发现的在BY和RM之间有表达差异的10个BY基因中的每个基因的启动子,并且在每种情况下,我们的定量PCR分析都揭示了启动子替换对基因表达的顺式效应。总之,我们的研究表明,反式作用因子在酵母菌株之间的表达进化中起主要作用,但顺式变异的作用也很重要。