Department of Genetics, University of Wisconsin-Madison, Madison, WI 53706.
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706.
Proc Natl Acad Sci U S A. 2020 Oct 27;117(43):26812-26821. doi: 10.1073/pnas.2013163117. Epub 2020 Oct 8.
The expression of genes encoding powerful developmental regulators is exquisitely controlled, often at multiple levels. Here, we investigate developmental expression of three conserved genes, , , and which encode homologs of ERK/MAPK and core components of the Notch-dependent transcription complex, respectively. We use single-molecule FISH (smFISH) and MATLAB to visualize and quantify nuclear nascent transcripts and cytoplasmic mRNAs as a function of position along the germline developmental axis. Using differentially labeled probes, one spanning an exceptionally long first intron and the other spanning exons, we identify two classes of active transcription sites (ATS). The iATS class, for "incomplete" ATS, harbors only partial nascent transcripts; the cATS class, for "complete" ATS, harbors full-length nascent transcripts. Remarkably, the frequencies of iATS and cATS are patterned along the germline axis. For example, most ATS are iATS in hermaphrodite germline stem cells, but most are cATS in differentiating stem cell daughters. Thus, ATS class frequencies switch in a graded manner as stem cell daughters begin differentiation. Importantly, the patterns of ATS class frequency are gene-, stage-, and sex-specific, and cATS frequency strongly correlates with transcriptional output. Although the molecular mechanism underlying ATS classes is not understood, their primary difference is the extent of transcriptional progression. To generate only partial nascent transcripts in iATS, progression must be slowed, paused, or aborted midway through the gene. We propose that regulation of ATS class can be a critical mode of developmental gene regulation.
基因表达的强大发育调节剂的编码是非常精确的控制,通常在多个层面上。在这里,我们研究三个保守的基因, , ,和 ,其编码分别为 ERK/MAPK 和 Notch 依赖的转录复合物的核心组件的同源物的发育表达。我们使用单分子 FISH ( smFISH )和 MATLAB 可视化和量化核新生转录物和细胞质 mRNA 的位置的功能沿生殖系发育轴。使用差异标记的探针,一个跨越一个非常长的第一内含子和另一个跨越外显子,我们确定了两类活性转录位点( ATS )。 iATS 类,为“不完整” ATS ,只含有部分新生转录物; cATS 类,为“完整” ATS ,含有全长新生转录物。值得注意的是, iATS 和 cATS 的频率沿生殖系轴形成图案。例如,大多数 ATS 在雌雄同体生殖干细胞中是 iATS ,但在分化的干细胞女儿中大多数是 cATS 。因此,随着干细胞女儿开始分化, ATS 类频率以渐变的方式切换。重要的是, ATS 类频率的模式是基因,阶段和性别特异性的,并且 cATS 频率与转录输出强烈相关。虽然 ATS 类的分子机制尚不清楚,但它们的主要区别是转录进展的程度。为了在 iATS 中仅产生部分新生转录物,进展必须在基因中间减速,暂停或中止。我们提出,ATS 类的调节可以是发育基因调节的关键模式。