The gene regulatory network controlling proximal limb development in mice

控制小鼠近端肢体发育的基因调控网络

• 批准号: RGPIN-2019-04812
• 负责人: Cobb, John
• 金额: $ 3.64万
• 依托单位: University of Calgary
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2021
• 资助国家: 加拿大
• 起止时间: 2021-01-01 至 2022-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=737877
• 关键词: gene; regulatory; network; controlling; proximal

The formation of specific structures in a developing embryo (embryonic patterning) requires that cells communicate by secreting signals that diffuse from one cell to another. Usually these signals are proteins. The genes of each cell contain a DNA code for these signalling proteins. These genes must be turned on and off precisely by other proteins called transcription factors. Transcription factors bind to DNA near genes to regulate how they are transcribed. Transcription is the process by which RNA is produced from the code of the DNA sequence and then RNA is then translated into proteins. Therefore, one of the biggest challenges of studying development is understanding how the genes that code for signalling proteins are turned on in specific cells by transcription factors and how the signalling proteins then direct the development of specific structures. In the short-term we focus on individual components of the embryonic patterning system so that we can later fit these modules into a larger system. Therefore, our long-term goal is to understand how genes are organized into more complex systems called gene regulatory networks. Within this context my laboratory studies the developmental function of the transcription factor SHOX2, which is encoded by the short stature homeobox gene 2 (Shox2). SHOX2 is an excellent model for understanding how a transcription factor controls development because it has an important function in a variety of developing structures including the limbs, palate, and heart . We have primarily studied how SHOX2 controls the development of specific bones of the limbs. We found that the humerus and femur of the arms and legs respectively are virtually deleted when the Shox2 gene is inactivated ("knocked out") during the development of the limbs. In the current proposal we use genetics (mating different kinds of mutant mice together) to determine how different genes work together to form limbs. We also propose to inactivate Shox2 in different cells in the limbs and at different times to tease apart when and where its function is important. Last, we also compare the mRNA from the limbs of different kinds of mutant mice to help determine which genes are regulated within the gene regulatory network that controls the development of the humerus and femur.

发育中的胚胎中特定结构的形成（胚胎图案）需要细胞通过分泌从一个细胞扩散到另一个细胞的信号来进行通信。通常这些信号是蛋白质。每个细胞的基因都包含这些信号蛋白的 DNA 代码。这些基因必须由称为转录因子的其他蛋白质精确地打开和关闭。转录因子与基因附近的 DNA 结合，调节基因的转录方式。转录是从 DNA 序列编码产生 RNA，然后 RNA 被翻译成蛋白质的过程。因此，研究发育的最大挑战之一是了解编码信号蛋白的基因如何在特定细胞中被转录因子打开，以及信号蛋白如何指导特定结构的发育。 在短期内，我们专注于胚胎模式系统的各个组件，以便我们以后可以将这些模块安装到更大的系统中。因此，我们的长期目标是了解基因如何组织成更复杂的系统（称为基因调控网络）。在此背景下，我的实验室研究转录因子 SHOX2 的发育功能，该因子由矮身材同源盒基因 2 (Shox2) 编码。 SHOX2 是了解转录因子如何控制发育的绝佳模型，因为它在包括四肢、上颚和心脏在内的各种发育结构中具有重要功能。我们主要研究了SHOX2如何控制四肢特定骨骼的发育。我们发现，当 Shox2 基因在四肢发育过程中失活（“敲除”）时，手臂和腿的肱骨和股骨实际上分别被删除。在当前的提案中，我们使用遗传学（将不同种类的突变小鼠交配在一起）来确定不同的基因如何协同工作以形成四肢。我们还建议在不同时间使四肢不同细胞中的 Shox2 失活，以区分其功能何时何地重要。最后，我们还比较了不同种类突变小鼠四肢的 mRNA，以帮助确定哪些基因在控制肱骨和股骨发育的基因调控网络中受到调控。