RNA binding proteins in cardiovascular development and disease.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Current Topics in Developmental Biology Pub Date : 2024-01-01 Epub Date: 2024-03-15 DOI:10.1016/bs.ctdb.2024.01.007
Sunil K Verma, Muge N Kuyumcu-Martinez
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Abstract

Congenital heart disease (CHD) is the most common birth defect affecting>1.35 million newborn babies worldwide. CHD can lead to prenatal, neonatal, postnatal lethality or life-long cardiac complications. RNA binding protein (RBP) mutations or variants are emerging as contributors to CHDs. RBPs are wizards of gene regulation and are major contributors to mRNA and protein landscape. However, not much is known about RBPs in the developing heart and their contributions to CHD. In this chapter, we will discuss our current knowledge about specific RBPs implicated in CHDs. We are in an exciting era to study RBPs using the currently available and highly successful RNA-based therapies and methodologies. Understanding how RBPs shape the developing heart will unveil their contributions to CHD. Identifying their target RNAs in the embryonic heart will ultimately lead to RNA-based treatments for congenital heart disease.

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心血管发育和疾病中的 RNA 结合蛋白
先天性心脏病(CHD)是最常见的出生缺陷,影响着全球 135 万以上的新生儿。先天性心脏病可导致产前、新生儿、产后死亡或终身心脏并发症。RNA结合蛋白(RBP)突变或变异正在成为CHD的诱因。RBP 是基因调控的奇才,是 mRNA 和蛋白质景观的主要贡献者。然而,人们对发育中的心脏中的 RBPs 及其对 CHD 的贡献知之甚少。在本章中,我们将讨论我们目前对与 CHD 有关的特定 RBPs 的了解。我们正处于一个激动人心的时代,可以利用目前可用且非常成功的基于 RNA 的疗法和方法来研究 RBPs。了解 RBPs 如何塑造发育中的心脏将揭示它们对 CHD 的贡献。确定它们在胚胎心脏中的靶 RNA 将最终导致基于 RNA 的先天性心脏病治疗方法。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
91
期刊最新文献
Cardiac construction-Recent advances in morphological and transcriptional modeling of early heart development. Computational approaches for mechanobiology in cardiovascular development and diseases. Genetics and etiology of congenital heart disease. Macrophage lineages in heart development and regeneration. RNA binding proteins in cardiovascular development and disease.
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