A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus. Academic Article uri icon

Overview

abstract

  • The factors driving or preventing pathological expansion of tandem repeats remain largely unknown. Here, we assessed the FGF14 (GAA)·(TTC) repeat locus in 2,530 individuals by long-read and Sanger sequencing and identified a common 5'-flanking variant in 70.34% of alleles analyzed (3,463/4,923) that represents the phylogenetically ancestral allele and is present on all major haplotypes. This common sequence variation is present nearly exclusively on nonpathogenic alleles with fewer than 30 GAA-pure triplets and is associated with enhanced stability of the repeat locus upon intergenerational transmission and increased Fiber-seq chromatin accessibility.

authors

  • Pellerin, David
  • Del Gobbo, Giulia F
  • Couse, Madeline
  • Dolzhenko, Egor
  • Nageshwaran, Sathiji
  • Cheung, Warren A
  • Xu, Isaac R L
  • Dicaire, Marie-Josée
  • Spurdens, Guinevere
  • Matos-Rodrigues, Gabriel
  • Stevanovski, Igor
  • Scriba, Carolin K
  • Rebelo, Adriana
  • Roth, Virginie
  • Wandzel, Marion
  • Bonnet, Céline
  • Ashton, Catherine
  • Agarwal, Aman
  • Peter, Cyril
  • Hasson, Dan
  • Tsankova, Nadejda M
  • Dewar, Ken
  • Lamont, Phillipa J
  • Laing, Nigel G
  • Renaud, Mathilde
  • Houlden, Henry
  • Synofzik, Matthis
  • Usdin, Karen
  • Nussenzweig, Andre
  • Napierala, Marek
  • Chen, Zhao
  • Jiang, Hong
  • Deveson, Ira W
  • Ravenscroft, Gianina
  • Akbarian, Schahram
  • Eberle, Michael A
  • Boycott, Kym M
  • Pastinen, Tomi
  • Brais, Bernard
  • Zuchner, Stephan
  • Danzi, Matt C

publication date

  • June 27, 2024

Research

keywords

  • Alleles
  • Fibroblast Growth Factors

Identity

PubMed Central ID

  • PMC11440897

Scopus Document Identifier

  • 85198753925

Digital Object Identifier (DOI)

  • 10.1038/s41588-024-01808-5

PubMed ID

  • 38937606

Additional Document Info

volume

  • 56

issue

  • 7