ResearchInnovation & Engagements Portfolio, Mangosuthu University of Technology, Durban, South Africa
ResearchInnovation & Engagements Portfolio, Mangosuthu University of Technology, Durban, South Africa.
J Mol Endocrinol. 2017 Aug;59(2):R93-R107. doi: 10.1530/JME-17-0049.
Diabetes mellitus (DM) is a non-communicable, metabolic disorder that affects 416 million individuals worldwide. Type 2 diabetes contributes to a vast 85-90% of the diabetes incidences while 10-15% of patients suffer from type 1 diabetes. These two predominant forms of DM cause a significant loss of functional pancreatic β-cell mass causing different degrees of insulin deficiency, most likely, due to increased β-cell apoptosis. Treatment options involve the use of insulin sensitisers, α-glucosidase inhibitors, and β-cell secretagogues which are often expensive, limited in efficacy and carry detrimental adverse effects. Cost-effective options for treatment exists in the form of herbal drugs, however, scientific validations of these widely used medicinal plants are still underway. Alternative splicing (AS) is a co-ordinated post-transcriptional process in which a single gene generates multiple mRNA transcripts which results in increased amounts of functionally different protein isoforms and in some cases aberrant splicing leads to metabolic disease. In this review, we explore the association of AS with metabolic alterations in DM and the biological significance of the abnormal splicing of some pathogenic diabetes-related genes. An understanding of the molecular mechanism behind abnormally spliced transcripts will aid in the development of new diagnostic, prognostic and therapeutic tools.
糖尿病(DM)是一种非传染性代谢紊乱疾病,影响着全球 4.16 亿人。2 型糖尿病占糖尿病发病率的 85-90%,而 10-15%的患者患有 1 型糖尿病。这两种主要形式的 DM 导致功能性胰腺β细胞大量丧失,导致不同程度的胰岛素缺乏,这很可能是由于β细胞凋亡增加所致。治疗方案包括使用胰岛素增敏剂、α-葡萄糖苷酶抑制剂和β细胞分泌剂,这些药物往往昂贵、疗效有限且有不良的副作用。以草药药物的形式存在着更具成本效益的治疗选择,但这些广泛使用的药用植物的科学验证仍在进行中。选择性剪接(AS)是一种协调的转录后过程,其中一个基因产生多个 mRNA 转录本,从而导致功能不同的蛋白质同工型的数量增加,在某些情况下,异常剪接导致代谢疾病。在这篇综述中,我们探讨了 AS 与 DM 代谢改变的关系,以及一些与发病相关的糖尿病基因异常剪接的生物学意义。了解异常剪接转录本背后的分子机制将有助于开发新的诊断、预后和治疗工具。