RAD51 haploinsufficiency causes congenital mirror movements in humans

Christel Depienne, Delphine Bouteiller, Aurélie Méneret, Ségolne Billot, Sergiu Groppa, Stephan Klebe, Fanny Charbonnier-Beaupel, Jean Christophe Corvol, Jean Paul Saraiva, Norbert Brueggemann, Kailash Bhatia, Massimo Cincotta, Vanessa Brochard, Constance Flamand-Roze, Wassila Carpentier, Sabine Meunier, Yannick Marie, Marion Gaussen, Giovanni Stevanin, Rosine WehrleMarie Vidailhet, Christine Klein, Isabelle Dusart, Alexis Brice*, Emmanuel Roze

*Corresponding author for this work
34 Citations (Scopus)


Congenital mirror movements (CMM) are characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side. CMM reflect dysfunctions and structural abnormalities of the motor network and are mainly inherited in an autosomal-dominant fashion. Recently, heterozygous mutations in DCC, the gene encoding the receptor for netrin 1 and involved in the guidance of developing axons toward the midline, have been identified but CMM are genetically heterogeneous. By combining genome-wide linkage analysis and exome sequencing, we identified heterozygous mutations introducing premature termination codons in RAD51 in two families with CMM. RAD51 mRNA was significantly downregulated in individuals with CMM resulting from the degradation of the mutated mRNA by nonsense-mediated decay. RAD51 was specifically present in the developing mouse cortex and, more particularly, in a subpopulation of corticospinal axons at the pyramidal decussation. The identification of mutations in RAD51, known for its key role in the repair of DNA double-strand breaks through homologous recombination, in individuals with CMM reveals a totally unexpected role of RAD51 in neurodevelopment. These findings open a new field of investigation for researchers attempting to unravel the molecular pathways underlying bimanual motor control in humans.

Original languageEnglish
JournalAmerican Journal of Human Genetics
Issue number2
Pages (from-to)301-307
Number of pages7
Publication statusPublished - 10.02.2012


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