Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance

Penelope E. Bonnen(Baylor College of Medicine), John W. Yarham(Wellcome Centre for Mitochondrial Research), Arnaud Besse(Baylor College of Medicine), Ping Chun Wu(Baylor College of Medicine), Eissa Faqeih(King Fahd Medical City), Ali Alasmari(King Fahd Medical City), Mohammad A.M. Saleh(King Fahd Medical City), Wafaa Eyaid(King Saud bin Abdulaziz University for Health Sciences), Alrukban Hadeel(King Saud bin Abdulaziz University for Health Sciences), Langping He(Wellcome Centre for Mitochondrial Research), Frances J.D. Smith(Guy's Hospital), Shu Yau(Guy's Hospital), Eve M. Simcox(Wellcome Centre for Mitochondrial Research), Satomi Miwa(Newcastle University), Taraka Donti(Baylor College of Medicine), Khaled K. Abu‐Amero(King Saud University), Lee‐Jun C. Wong(Baylor College of Medicine), William J. Craigen(Baylor College of Medicine), Brett H. Graham(Baylor College of Medicine), Kenneth L. Scott(Baylor College of Medicine), Robert McFarland(Wellcome Centre for Mitochondrial Research), Robert W. Taylor(Wellcome Centre for Mitochondrial Research)
The American Journal of Human Genetics
August 29, 2013
Cited by 178Open Access
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Abstract

Nuclear genetic disorders causing mitochondrial DNA (mtDNA) depletion are clinically and genetically heterogeneous, and the molecular etiology remains undiagnosed in the majority of cases. Through whole-exome sequencing, we identified recessive nonsense and splicing mutations in FBXL4 segregating in three unrelated consanguineous kindreds in which affected children present with a fatal encephalopathy, lactic acidosis, and severe mtDNA depletion in muscle. We show that FBXL4 is an F-box protein that colocalizes with mitochondria and that loss-of-function and splice mutations in this protein result in a severe respiratory chain deficiency, loss of mitochondrial membrane potential, and a disturbance of the dynamic mitochondrial network and nucleoid distribution in fibroblasts from affected individuals. Expression of the wild-type FBXL4 transcript in cell lines from two subjects fully rescued the levels of mtDNA copy number, leading to a correction of the mitochondrial biochemical deficit. Together our data demonstrate that mutations in FBXL4 are disease causing and establish FBXL4 as a mitochondrial protein with a possible role in maintaining mtDNA integrity and stability.


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