Stability of Mosaic Divergent Repeat Interruptions in X‐Linked Dystonia‐Parkinsonism

Author:

Laß Joshua1ORCID,Lüth Theresa1,Schlüter Kathleen1,Schaake Susen1,Laabs Björn‐Hergen2,Much Christoph1,Jamora Roland Dominic3ORCID,Rosales Raymond L.4,Saranza Gerard5ORCID,Diesta Cid Czarina E.6,Pearson Christopher E.7,König Inke R.2,Brüggemann Norbert18,Klein Christine1,Westenberger Ana1,Trinh Joanne1

Affiliation:

1. Institute of Neurogenetics, University of Lübeck Lübeck Germany

2. Institute of Medical Biometry and Statistics, University of Lübeck Lübeck Germany

3. Department of Neurosciences College of Medicine‐Philippine General Hospital, University of the Philippines Manila Manila Philippines

4. Department of Neurology and Psychiatry University of Santo Tomas and the CNS‐Metropolitan Medical Center, Manila, Philippines Section of Neurology Manila Philippines

5. Department of Internal Medicine Chong Hua Hospital Cebu Philippines

6. Department of Neurosciences Movement Disorders Clinic, Makati Medical Center Makati City Philippines

7. Department of Molecular Genetics University of Toronto Toronto Canada

8. Department of Neurology University of Lübeck Lübeck Germany

Abstract

AbstractBackgroundX‐Linked dystonia‐parkinsonism (XDP) is an adult‐onset neurodegenerative disorder characterized by rapidly progressive dystonia and parkinsonism. Mosaic Divergent Repeat Interruptions affecting motif Length and Sequence (mDRILS) were recently found within the TAF1 SVA repeat tract and were shown to associate with repeat stability and age at onset in XDP, specifically the AGGG [5′‐SINE‐VNTR‐Alu(AGAGGG)2AGGG(AGAGGG)n] mDRILS.ObjectiveThis study aimed to investigate the stability of mDRILS frequencies and stability of (AGAGGG)n repeat length during transmission in parent–offspring pairs.MethodsFifty‐six families (n = 130) were investigated for generational transmission of repeat length and mDRILS. The mDRILS stability of 16 individuals was assessed at two sampling points 1 year apart. DNA was sequenced with long‐read technologies after long‐range polymerase chain reaction amplification of the TAF1 SVA. Repeat number and mDRILS were detected with Noise‐Cancelling Repeat Finder (NCRF).ResultsWhen comparing the repeat domain, 51 of 65 children had either contractions or expansions of the repeat length. The AGGG frequency remained stable across generations at 0.074 (IQR: 0.069–0.078) (z = −0.526; P = 0.599). However, the median AGGG frequency in children with an expansion (0.072 [IQR: 0.066–0.076]) was lower compared with children with retention or contraction (0.080 [IQR: 0.073–0.083]) (z = −0.007; P = 0.003). In a logistic regression model, the AGGG frequency predicted the outcome of either expansion or retention/contraction when including repeat number and sex as covariates (β = 80.7; z‐score = 2.63; P = 0.0085). The AGGG frequency varied slightly over 1 year (0.070 [IQR: 0.063–0.080] to 0.073 [IQR: 0.069–0.078]).ConclusionsOur results show that a higher AGGG frequency may stabilize repeats across generations. This highlights the importance of further investigating mDRILS as a disease‐modifying factor with generational differences. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Deutsche Forschungsgemeinschaft

Canadian Institutes of Health Research

Peter und Traudl Engelhorn Stiftung

Publisher

Wiley

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