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人类序列形成R环结构。

Human sequences form R-loop structures .

作者信息

Parsons Agata M, Su Kemin, Daniels Maya, Bouma Gerrit J, Vanden Heuvel Gregory B, Larson Erik D

机构信息

Biomedical Sciences, Western Michigan University Homer Stryker MD School of Medicine, Kalamazoo, Michigan, United States.

Investigative Medicine, Western Michigan University Homer Stryker MD School of Medicine, Kalamazoo, Michigan, United States.

出版信息

MicroPubl Biol. 2024 Feb 2;2024. doi: 10.17912/micropub.biology.001058. eCollection 2024.

Abstract

Autosomal dominant polycystic kidney disease results from the loss of the gene product, polycystin 1. Regulatory mechanisms are unresolved, but an apparent G/C sequence bias in the gene is consistent with co-transcriptional R-loop formation. R-loops regulate gene expression and stability, and they form when newly synthesized RNA extensively pairs with the template DNA to displace the non-template strand. In this study, we tested two human sequences for co-transcriptional R-loop formation in vitro. We observed RNase H-sensitive R-loop formation in intron 1 and 22 sequences, but only in one transcriptional orientation. Therefore, R-loops may participate in expression or stability.

摘要

常染色体显性多囊肾病是由于基因产物多囊蛋白1缺失所致。调控机制尚未明确,但该基因中明显的G/C序列偏向与共转录R环形成一致。R环调节基因表达和稳定性,当新合成的RNA与模板DNA广泛配对以取代非模板链时形成。在本研究中,我们在体外测试了两个人类序列的共转录R环形成。我们在第1内含子和第22序列中观察到了对核糖核酸酶H敏感的R环形成,但仅在一个转录方向上。因此,R环可能参与了基因表达或稳定性的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/373b/10873753/4554df4d06d7/25789430-2024-micropub.biology.001058.jpg

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