Department of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA, USA.
Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA, USA.
RNA Biol. 2024 Jan;21(1):39-51. doi: 10.1080/15476286.2024.2417155. Epub 2024 Oct 21.
Although long noncoding RNAs (lncRNAs) constitute the majority of the human transcriptome, the functional roles of most remain elusive. While protein-coding genes in macrophage biology have been extensively studied, the contribution of lncRNAs in this context is poorly understood. Given the vast number of lncRNAs (>20,000), identifying candidates for functional characterization poses a significant challenge. Here, we present two complementary approaches to pinpoint and investigate lncRNAs involved in monocyte-to-macrophage differentiation: RNA-seq for functional inference and a high-throughput functional screen. These strategies enabled us to identify four lncRNA regulators of monocyte differentiation: , , , and . Preliminary insights suggest these lncRNAs may act in through neighbouring protein-coding genes, although their precise mechanisms remain to be elucidated. We further discuss the strengths and weaknesses of these methodologies, along with validation pipelines crucial for establishing lncRNA functionality.
尽管长链非编码 RNA(lncRNA)构成了人类转录组的大部分,但大多数的功能作用仍难以捉摸。尽管巨噬细胞生物学中的蛋白编码基因已经得到了广泛的研究,但在这种情况下,lncRNA 的贡献还知之甚少。鉴于 lncRNA 的数量庞大(>20000),确定具有功能特征的候选者是一个重大挑战。在这里,我们提出了两种互补的方法来确定和研究参与单核细胞向巨噬细胞分化的 lncRNA:RNA-seq 用于功能推断和高通量功能筛选。这些策略使我们能够鉴定出四个调节单核细胞分化的 lncRNA:,,, 和.初步的见解表明,这些 lncRNA 可能通过邻近的蛋白编码基因在 中发挥作用,尽管它们的确切机制仍有待阐明。我们还讨论了这些方法的优缺点,以及对于建立 lncRNA 功能至关重要的验证管道。