Walker Amy K, Boag Peter R, Blackwell T Keith
Section on Developmental and Stem Cell Biology, Joslin Diabetes Center, Department of Pathology, Harvard Medical School, Harvard Stem Cell Institute, One Joslin Place, Boston, MA 02215, USA.
Dev Biol. 2007 Apr 1;304(1):382-93. doi: 10.1016/j.ydbio.2006.12.039. Epub 2006 Dec 23.
Developing oocytes produce materials that will support early embryonic development then cease transcription before fertilization. Later, a distinct transcription program is established in the embryo. Little is understood about how these global gene regulation transitions are effected. We have investigated in C. elegans how oocyte transcription is influenced by maturation, a process that releases meiotic arrest and prepares for fertilization. By monitoring transcription-associated phosphorylation of the RNA polymerase II (Pol II) C-terminal domain (CTD), we find that oocyte transcription shuts down independently of maturation. Surprisingly, maturation signals then induce CTD phosphorylation that is associated specifically with transcription initiation steps and accumulates to high levels when expression of the CTD phosphatase FCP-1 is inhibited. This CTD phosphorylation is also uncovered when a ubiquitylation pathway is blocked, or when maturation is stimulated precociously. CTD phosphorylation is similarly detected during embryonic mitosis, when transcription is also largely silenced. We conclude that oocyte maturation signals induce abortive transcription events in which FCP-1 may recycle phosphorylated Pol II and that analogous processes may occur during mitosis. Our findings suggest that maturation signals may initiate preparations for embryonic transcription, possibly as part of a broader program that begins the transition from maternal to zygotic gene expression.
发育中的卵母细胞产生支持早期胚胎发育的物质,然后在受精前停止转录。之后,胚胎中会建立一个独特的转录程序。对于这些全局基因调控转变是如何发生的,我们了解甚少。我们在秀丽隐杆线虫中研究了卵母细胞转录如何受到成熟过程的影响,成熟过程会解除减数分裂阻滞并为受精做准备。通过监测RNA聚合酶II(Pol II)C末端结构域(CTD)的转录相关磷酸化,我们发现卵母细胞转录的关闭与成熟无关。令人惊讶的是,成熟信号随后诱导CTD磷酸化,这与转录起始步骤特异性相关,并且当CTD磷酸酶FCP - 1的表达受到抑制时会积累到高水平。当泛素化途径被阻断或成熟被过早刺激时,也会出现这种CTD磷酸化。在胚胎有丝分裂期间,当转录也基本沉默时,同样检测到CTD磷酸化。我们得出结论,卵母细胞成熟信号诱导流产性转录事件,其中FCP - 1可能循环利用磷酸化的Pol II,并且类似的过程可能在有丝分裂期间发生。我们的研究结果表明,成熟信号可能启动胚胎转录的准备工作,这可能是从母源基因表达向合子基因表达转变的更广泛程序的一部分。