Mechanisms of gene expression

转录调控是细胞协调单个基因或一组基因表达的手段。最近对单细胞的研究表明，在大多数情况下，转录不是一种连续的活动，而是以爆发的形式发生。每个基因产生的核糖核糖核酸的量与这种爆发的幅度和频率成正比。这两个参数是如何控制的还不完全清楚，但似乎启动子上的DNA序列信息决定了幅度，而猝发频率取决于增强子上的序列信息。启动子和增强子也被称为基因调控元件。它们的主要作用是招募酶(聚合酶)和其他关键蛋白质(转录因子、激活剂和抑制物)，打开DNA螺旋并读取遗传信息。启动子和增强子的另一个重要特征是，为了正常发挥作用，它们必须紧密接近或相互接触。这些相互作用不仅对基因表达很重要，而且正如我们的实验室和其他实验室在过去5年中所表明的那样，它们是对免疫系统至关重要的基因重组的关键。本财年，我们的实验室继续探索细胞如何促进调控DNA之间的联系，以推动淋巴细胞的转录和重组。 这一领域的主要出版物： 1-Zhang et al.《自然》，2019年11月和巴等人。《自然》，2020年7月。在这些手稿中，我们与哈佛大学的弗雷德·阿尔特合作表明，抗体基因的重组是由核结构蛋白、CTCF和粘附素驱动的。它们的活性确保了B细胞表达广泛的抗体受体，在感染过程中可以识别病原体。 2-Senigl等人。《细胞报告》，2019年12月。在这篇手稿中，我们与David Schatz(耶鲁大学)合作报道了核结构促进抗体受体基因的突变。这一过程确保抗原(病原体)在感染期间以极高的亲和力被识别。 3-Liu et al.《细胞研究》，2020年4月。在这份报告中，我们描述了一种名为ERCC6L2的DNA修复蛋白在解决抗体基因重组中间的DNA断裂中的作用。 4-Xie等人。《自然方法》，2020年4月。本文报道了一种新的显微技术，它可以可视化哺乳动物基因组中的转录活性区域。

Transcriptional regulation is the means whereby cells orchestrate expression of individual genes or group of genes. Recent studies with single cells have shown that, for the most part, transcription is not a continuous activity but it occurs in bursts. The amount of RNA produced for each gene is directly proportional to the amplitude and frequency of such bursts. How these two parameters are controlled is not totally clear, but it appears that DNA sequence information at promoters determine the amplitude, while burst frequencies rely on sequence information at enhancers. Promoters and enhancers are also known as gene regulatory elements. Their primary role is to recruit enzymes (polymerases) and other key proteins (transcription factors, activators and inhibitors) that open up the DNA helix and read the genetic information. Another important feature of promoters and enhancers is that to function properly they must either be in close proximity or in contact with each other. These interactions are not only important for gene expression, but as our laboratoratory and others have shown in the past 5 years, they are key to recombination of genes key for the immune system. This fiscal year, our laboratory has continue exploring how the cell facilitate contacts between regulatory DNA to drive transcription and recombination in lymphocytes. Key publications in this area: 1- Zhang et al. Nature, November 2019 and Ba et al. Nature, July 2020. In these manuscripts we have shown in collaboration with Fred Alt (Harvard) that recombination of antibody genes is driven by nuclear architectural proteins CTCF and cohesin. Their activity ensures that B cells express a broad range of antibody receptors with which pathogens are recognized during infection. 2- Senigl et al. Cell Reports, December 2019. In this manuscript we reported in collaboration with David Schatz (Yale) that nuclear architecture facilitates the mutation of antibody receptor genes. This process ensures that antigens (pathogens) are recognized with exquisite affinity during an infection. 3- Liu et al. Cell Research, April 2020. In this report we characterized the role of a DNA repair protein, known as ERCC6L2, in the resolution of DNA breaks intermediate to antibody gene recombination. 4- Xie et al. Nature Methods, April 2020. This paper reports a new microscopy technique that permits visualization of transcriptionally active domains in the mammalian genome.