Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism

Author:

Dawidziuk Mateusz,Podwysocka Aleksandra,Jurek Marta,Obersztyn Ewa,Bekiesinska-Figatowska Monika,Goszczanska-Ciuchta Alicja,Bukowska-Olech Ewelina,Rygiel Agnieszka Magdalena,Guilbride Dorothy Lys,Wiszniewski Wojciech,Gawlinski PawelORCID

Abstract

AbstractCoenzyme Q5 (COQ5), a C-methyltransferase, modifies coenzyme Q10 (COQ10) during biosynthesis and interacts with polyA-tail regulating zinc-finger protein ZC3H14 in neural development. Here, we present a fifth patient (a third family) worldwide with neurodevelopmental and physiological symptoms including COQ10 deficiency. Our patient harbors one novel c.681+1G>A and one recurrent p.Gly118Ser variant within COQ5. The patient’s mRNA profile reveals multiple COQ5 splice-variants. Subsequently, we comprehensively described patient’s clinical features as compared to phenotype and symptoms of other known congenital coenzyme Q5-linked cases. A core spectrum of COQ5-associated symptoms includes reduced COQ10 levels, intellectual disability, encephalopathy, cerebellar ataxia, cerebellar atrophy speech regression/dysarthria, short stature, and developmental delays. Our patient additionally displays dysmorphia, microcephaly, and regressive social faculties. These results formally establish causal association of biallelic COQ5 mutation with pathology, outline a core COQ5-linked phenotype, and identify mRNA mis-splicing as the molecular mechanism underlying all COQ5 variant-linked pathology to date.

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

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