Christchurch Heart Institute, University of Otago, Christchurch 8011, New Zealand.
School of Natural and Computational Sciences, Massey University, Auckland 0745, New Zealand.
Int J Mol Sci. 2021 Oct 20;22(21):11324. doi: 10.3390/ijms222111324.
Long noncoding RNAs (lncRNAs) have been implicated in the pathogenesis of cardiovascular diseases. We aimed to identify novel lncRNAs associated with the early response to ischemia in the heart.
RNA sequencing data gathered from 81 paired left ventricle samples from patients undergoing cardiopulmonary bypass was collected before and after a period of ischemia. Novel lncRNAs were validated with Oxford Nanopore Technologies long-read sequencing. Gene modules associated with an early ischemic response were identified and the subcellular location of selected lncRNAs was determined with RNAscope. A total of 2446 mRNAs, 270 annotated lncRNAs and one novel lncRNA differed in response to ischemia (adjusted < 0.001, absolute fold change >1.2). The novel lncRNA belonged to a gene module of highly correlated genes that also included 39 annotated lncRNAs. This module associated with ischemia (Pearson correlation coefficient = -0.69, = 1 × 10) and activation of cell death pathways ( < 6 × 10). A further nine novel cardiac lncRNAs were identified, of which, one overlapped five cis-eQTL eSNPs for the gene RWD Domain-Containing Sumoylation Enhancer (RWDD3) and was itself correlated with RWDD3 expression (Pearson correlation coefficient -0.2, = 0.002).
We have identified 10 novel lncRNAs, one of which was associated with myocardial ischemia and may have potential as a novel therapeutic target or early marker for myocardial dysfunction.
长链非编码 RNA(lncRNA)与心血管疾病的发病机制有关。我们旨在鉴定与心脏缺血早期反应相关的新型 lncRNA。
从 81 例接受体外循环的患者的 81 对左心室样本中收集了 RNA 测序数据,这些数据在缺血前后采集。使用牛津纳米孔技术长读测序验证新型 lncRNA。鉴定与早期缺血反应相关的基因模块,并通过 RNAscope 确定选定 lncRNA 的亚细胞位置。共有 2446 个 mRNAs、270 个注释 lncRNA 和一个新型 lncRNA 对缺血有反应(调整后 <0.001,绝对倍数变化 >1.2)。新型 lncRNA 属于一个高度相关基因的基因模块,该模块还包括 39 个注释 lncRNA。该模块与缺血(皮尔逊相关系数 =-0.69, = 1×10)和细胞死亡途径的激活相关( <6×10)。还鉴定了另外 9 个新型心脏 lncRNA,其中一个与 RWD 结构域包含 SUMOylation Enhancer(RWDD3)基因的 5 个顺式-eQTL eSNP 重叠,并且本身与 RWDD3 表达相关(皮尔逊相关系数 -0.2, = 0.002)。
我们已经鉴定了 10 个新型 lncRNA,其中一个与心肌缺血相关,可能具有作为新型治疗靶点或心肌功能障碍的早期标志物的潜力。