Longitudinal intronic RNA-Seq analysis of Parkinson's disease patients reveals disease-specific nascent transcription.

Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004 and Quinn, John P ORCID: 0000-0003-3551-7803
(2022) Longitudinal intronic RNA-Seq analysis of Parkinson's disease patients reveals disease-specific nascent transcription. Experimental biology and medicine (Maywood, N.J.). 15353702221081027 - 15353702221081027.

[img] Text
IntronicTranscritpionParkinsonKoks_EBMsubmission24012022_MedRXIV_version3.pdf - Accepted Version

Download (908kB) | Preview


Transcriptomic studies usually focus on either gene or exon-based annotations, and only limited experiments have reported changes in reads mapping to introns. The analysis of intronic reads allows the detection of nascent transcription that is not influenced by steady-state RNA levels and provides information on actively transcribed genes. Here, we describe substantial intronic transcriptional changes in Parkinson's disease (PD) patients compared to healthy controls (CO) at two different timepoints; at the time of diagnosis (BL) and three years later (V08). We used blood RNA-Seq data from the Parkinson's Progression Markers Initiative (PPMI) cohort and identified significantly changed transcription of intronic reads only in PD patients during this follow-up period. In CO subjects, only nine transcripts demonstrated differentially expressed introns between visits. However, in PD patients, 4873 transcripts had differentially expressed introns at visit V08 compared to BL, many of them in genes previously associated with neurodegenerative diseases, such as <i>LRRK2</i>, <i>C9orf72</i>, <i>LGALS3</i>, <i>KANSL1AS1</i>, and <i>ALS2</i>. In addition, at the time of diagnosis (BL visit), we identified 836 transcripts (e.g. <i>SNCA</i>, <i>DNAJC19</i>, <i>PRRG4</i>) and at visit V08, 2184 transcripts (e.g. <i>PINK1</i>, <i>GBA</i>, <i>ALS2</i>, <i>PLEKHM1</i>) with differential intronic expression specific to PD patients. In contrast, reads mapping to exonic regions demonstrated little variation indicating highly specific changes only in intronic transcription. Our study demonstrated that PD is characterized by substantial changes in the nascent transcription, and description of these changes could help to understand the molecular pathology underpinning this disease.

Item Type: Article
Divisions: Faculty of Health and Life Sciences
Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology
Depositing User: Symplectic Admin
Date Deposited: 24 Mar 2022 10:42
Last Modified: 07 Sep 2022 20:12
DOI: 10.1177/15353702221081027
URI: https://livrepository.liverpool.ac.uk/id/eprint/3151401