Jaynes James B, Fujioka Miki
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Dev Biol. 2004 May 15;269(2):609-22. doi: 10.1016/j.ydbio.2004.03.001.
The pair-rule segmentation gene even skipped (eve) is required to activate engrailed stripes and to organize odd-numbered parasegments (PSs). The protein product Eve has been shown to be an active repressor of transcription, and recent models for Eve function suggest that activation of engrailed is indirect, but these models have not been fully tested. Here we identify the forkhead domain transcription factor Sloppy-paired as the key intermediate in the initial activation of engrailed by Eve in odd-numbered parasegments. We also analyze the roles of the transcription factors Runt and Odd-skipped in this process. Detailed analysis of engrailed and pair-rule gene expression in various mutant combinations shows how eve activates engrailed by repressing these engrailed repressors, and further indicates that mutual repression among pair-rule genes plays an important role in establishing parasegment boundaries. We present a new model of pair-rule gene function that explains the response of these boundaries to the relative levels of Eve and Fushi Tarazu.
配对规则分割基因“偶数缺失”(eve)对于激活 engrailed 条纹和组织奇数副节(PSs)是必需的。Eve 蛋白产物已被证明是一种活跃的转录抑制因子,最近关于 Eve 功能的模型表明 engrailed 的激活是间接的,但这些模型尚未得到充分验证。在这里,我们确定叉头结构域转录因子 Sloppy-paired 是 Eve 在奇数副节中对 engrailed 进行初始激活的关键中间体。我们还分析了转录因子 Runt 和 Odd-skipped 在这一过程中的作用。对各种突变组合中 engrailed 和配对规则基因表达的详细分析表明,eve 如何通过抑制这些 engrailed 抑制因子来激活 engrailed,并进一步表明配对规则基因之间的相互抑制在建立副节边界中起着重要作用。我们提出了一个新的配对规则基因功能模型,该模型解释了这些边界对 Eve 和 Fushi Tarazu 相对水平的反应。