Department of Clinical Pharmacology and Flinders Cancer Centre, Flinders University, College of Medicine and Public Health, Flinders Medical Centre, Bedford Park, South Australia, Australia
Department of Clinical Pharmacology and Flinders Cancer Centre, Flinders University, College of Medicine and Public Health, Flinders Medical Centre, Bedford Park, South Australia, Australia.
Mol Pharmacol. 2021 Jun;99(6):488-503. doi: 10.1124/molpharm.120.000225. Epub 2021 Apr 6.
The human UDP-glycosyltransferase () gene superfamily generates 22 canonical transcripts coding for functional enzymes and also produces nearly 150 variant UGT transcripts through alternative splicing and intergenic splicing. In the present study, our analysis of circRNA databases identified backsplicing events that predicted 85 circRNAs from genes, with 33, 11, and 19 circRNAs from , , , respectively. Most of these UGT circRNAs were reported by one database and had low abundance in cell- or tissue-specific contexts. Using reverse-transcriptase polymerase chain reaction with divergent primers and cDNA samples from human tissues and cell lines, we found 13 circRNAs from four genes: (three), (one), (one), and (eight). Notably, all eight UGT8 circRNAs contain open reading frames that include the canonical start AUG codon and encode variant proteins that all have the common 274-amino acidN-terminal region of wild-type UGT8 protein. We further showed that one UGT8 circRNA (circ_UGT8-1) was broadly expressed in human tissues and cell lines, resistant to RNase R digestion, and predominately present in the cytoplasm. We cloned five UGT8 circRNAs into the Zinc finger with KRAB and SCAN domains 1 vector and transfected them into HEK293T cells. All these vectors produced both circRNAsand linear transcripts with varying circular/linear ratios (0.17-1.14).Western blotting and mass spectrometry assays revealed that only linear transcripts and not circRNAs were translated. In conclusion, our findings of nearly 100 circRNAs greatly expand the complexity and diversity of the UGT transcriptome; however, UGT circRNAs are expressed at a very low level in specific cellular contexts, and their biologic functions remain to be determined. SIGNIFICANCE STATEMENT: The human UGT gene transcriptome comprises 22 canonical transcripts coding for functional enzymes and approximately 150 alternatively spliced and chimeric variant transcripts. The present study identified nearly 100 circRNAs from genes, thus greatly expanding the complexity and diversity of the UGT transcriptome. UGT circRNAs were expressed broadly in human tissues and cell lines; however, most showed very low abundance in tissue- and cell-specific contexts, and therefore their biological functions remain to be investigated.
人类 UDP-糖基转移酶(UGT)基因超家族产生 22 种规范转录本,编码功能酶,并且还通过选择性剪接和基因间剪接产生近 150 种变异 UGT 转录本。在本研究中,我们对环状 RNA 数据库的分析鉴定了反向剪接事件,这些事件预测了 85 种来自 基因的环状 RNA,分别来自 、 、 。这些 UGT 环状 RNA 中的大多数仅被一个数据库报道,并且在细胞或组织特异性背景中丰度较低。使用具有发散引物的逆转录酶聚合酶链反应和来自人组织和细胞系的 cDNA 样本,我们从四个 基因中发现了 13 种环状 RNA: (三种)、 (一种)、 (一种)和 (八种)。值得注意的是,所有 8 种 UGT8 环状 RNA 均包含开放阅读框,其中包括规范的起始 AUG 密码子,并编码具有野生型 UGT8 蛋白的共同 274 个氨基酸 N 端区域的变异蛋白。我们进一步表明,一种 UGT8 环状 RNA(circ_UGT8-1)在人组织和细胞系中广泛表达,对核糖核酸酶 R 消化具有抗性,并且主要存在于细胞质中。我们将 5 种 UGT8 环状 RNA 克隆到锌指结构域 1 载体中,并将其转染到 HEK293T 细胞中。所有这些载体均产生环状 RNA 和线性转录本,其环状/线性比值不同(0.17-1.14)。Western 印迹和质谱分析显示,只有线性转录本而不是环状 RNA 被翻译。总之,我们发现的近 100 种环状 RNA 极大地扩展了 UGT 转录组的复杂性和多样性;然而,在特定的细胞环境中,UGT 环状 RNA 的表达水平非常低,其生物学功能仍有待确定。
人类 UGT 基因转录组包括 22 种规范转录本,编码功能酶,以及大约 150 种选择性剪接和嵌合变异转录本。本研究从 基因中鉴定了近 100 种环状 RNA,从而极大地扩展了 UGT 转录组的复杂性和多样性。UGT 环状 RNA 在人组织和细胞系中广泛表达;然而,大多数在组织和细胞特异性背景中丰度非常低,因此其生物学功能仍有待研究。