19-BBSRC-NSF/BIO: Inference of isoform-level regulatory infrastructures with studies in steroid-producing cell

19-BBSRC-NSF/BIO：通过类固醇生成细胞的研究推断异构体水平的调控基础设施

• 批准号: BB/V006126/1
• 负责人: Bidesh Mahata
• 金额: $ 31.57万
• 依托单位: University of Cambridge
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2020
• 资助国家: 英国
• 起止时间: 2020 至 无数据
• 项目状态: 未结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FV006126%2F1
• 关键词: 19; BBSRC; NSF; BIO; Inference

Cells are the fundamental units that provide all functions needed to sustain life in living organisms. Cellular functions are carried out by proteins, products of genes and the process of producing proteins from genes (i.e., gene expression) is mediated by a complex regulation system. Much remains unknown about the mechanism of gene regulation. Given all genes in a cell, the regulatory relationships between them can be represented by a network, called gene regulatory network. It has been a long-standing challenge to reconstruct these networks experimentally and computationally. A gene can express multiple isoforms (mRNA molecules), and hence produce multiple different proteins, which makes the underlying gene regulatory network more complicated. This project aims to computationally reconstruct accurate regulatory networks at the isoform-level from large-scale sequencing data. The project will first develop efficient approaches to identify the expressed isoforms and to determine their expression abundances, and then develop a network-reconstruction method which improves over the current status. The new computational methods will be validated and applied to the field of immunology--to study cellular mechanisms in steroid-producing cells. The project will contribute to both computer science and biology. The computational problems formulated consider an important problem in biology (infer the regulatory mechanisms of gene expression), and the formulated computational tasks bring new challenges to computer science and mathematics. The project will provide a toolkit to study the immune cell-mediated steroidogenesis pathway in cancer and reveal basic principles of steroid biosynthesis in tumour-infiltrating immune cells. The research can be integrated with educational activities and outreach, such as courses on topics of algorithms in computational biology. The software and data produced in this project will be made easily accessible to the public.

细胞是提供生物体维持生命所需的所有功能的基本单位。细胞功能是由蛋白质、基因产物来实现的，而由基因产生蛋白质的过程（即基因表达）是由一个复杂的调控系统介导的。关于基因调控的机制仍有许多未知之处。给定细胞中所有的基因，它们之间的调控关系可以用一个网络来表示，称为基因调控网络。通过实验和计算重建这些网络一直是一个长期的挑战。一个基因可以表达多个同种异构体（mRNA分子），从而产生多种不同的蛋白质，这使得潜在的基因调控网络更加复杂。该项目旨在从大规模测序数据中计算重建精确的同工异构体水平调控网络。该项目将首先开发有效的方法来识别表达的同种异构体并确定其表达丰度，然后开发一种网络重建方法，以改进目前的状况。新的计算方法将被验证并应用于免疫学领域——研究类固醇产生细胞的细胞机制。这个项目将对计算机科学和生物学都有贡献。公式化的计算问题考虑了生物学中的一个重要问题（推断基因表达的调控机制），公式化的计算任务给计算机科学和数学带来了新的挑战。该项目将为研究肿瘤中免疫细胞介导的类固醇生成途径和揭示肿瘤浸润免疫细胞中类固醇生物合成的基本原理提供工具箱。这项研究可以与教育活动和外展活动相结合，例如关于计算生物学中算法主题的课程。在这个项目中产生的软件和数据将很容易地提供给公众。

项目成果

Revisiting steroidogenesis and its role in immune regulation with the advanced tools and technologies.

• DOI: 10.1038/s41435-021-00139-3
• 发表时间: 2021-07
• 期刊: Genes and immunity
• 影响因子: 5
• 作者: Chakraborty S;Pramanik J;Mahata B
• 通讯作者: Mahata B