Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/92072
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dc.contributor.authorJolly, L.en
dc.contributor.authorNguyen, L.en
dc.contributor.authorDomingo, D.en
dc.contributor.authorSun, Y.en
dc.contributor.authorBarry, S.en
dc.contributor.authorHancarova, M.en
dc.contributor.authorPlevova, P.en
dc.contributor.authorVlckova, M.en
dc.contributor.authorHavlovicova, M.en
dc.contributor.authorKalscheuer, V.en
dc.contributor.authorGraziano, C.en
dc.contributor.authorPippucci, T.en
dc.contributor.authorBonora, E.en
dc.contributor.authorSedlacek, Z.en
dc.contributor.authorGecz, J.en
dc.date.issued2015en
dc.identifier.citationHuman Molecular Genetics, 2015; 24(12):3335-3347en
dc.identifier.issn1460-2083en
dc.identifier.issn1460-2083en
dc.identifier.urihttp://hdl.handle.net/2440/92072-
dc.description.abstractBoth gain- and loss-of-function mutations have recently implicated HCFC1 in neurodevelopmental disorders. Here, we extend our previous HCFC1 over-expression studies by employing short hairpin RNA to reduce the expression of Hcfc1 in embryonic neural cells. We show that in contrast to over-expression, loss of Hcfc1 favoured proliferation of neural progenitor cells at the expense of differentiation and promoted axonal growth of post-mitotic neurons. To further support the involvement of HCFC1 in neurological disorders, we report two novel HCFC1 missense variants found in individuals with intellectual disability (ID). One of these variants, together with three previously reported HCFC1 missense variants of unknown pathogenicity, were functionally assessed using multiple cell-based assays. We show that three out of the four variants tested result in a partial loss of HCFC1 function. While over-expression of the wild-type HCFC1 caused reduction in HEK293T cell proliferation and axonal growth of neurons, these effects were alleviated upon over-expression of three of the four HCFC1 variants tested. One of these partial loss-of-function variants disrupted a nuclear localization sequence and the resulting protein displayed reduced ability to localize to the cell nucleus. The other two variants displayed negative effects on the expression of the HCFC1 target gene MMACHC, which is responsible for the metabolism of cobalamin, suggesting that these individuals may also be susceptible to cobalamin deficiency. Together, our work identifies plausible cellular consequences of missense HCFC1 variants and identifies likely and relevant disease mechanisms that converge on embryonic stages of brain developmenten
dc.description.statementofresponsibilityLachlan A. Jolly, Lam Son Nguyen, Deepti Domingo, Ying Sun, Simon Barry, Miroslava Hancarova, Pavlina Plevova, Marketa Vlckova, Marketa Havlovicova, Vera M. Kalscheuer, Claudio Graziano, Tommaso Pippucci, Elena Bonora, Zdenek Sedlacek, and Jozef Geczen
dc.language.isoenen
dc.publisherOxford University Press (OUP)en
dc.rights© The Author 2015.en
dc.subjectBrain; Cells, Cultured; Animals; Humans; Mice; Carrier Proteins; RNA, Small Interfering; Transduction, Genetic; Amino Acid Substitution; Pedigree; Cell Differentiation; Cell Proliferation; Gene Expression; RNA Interference; Amino Acid Sequence; Active Transport, Cell Nucleus; Mutation; Female; Male; Host Cell Factor C1; HEK293 Cells; Neural Stem Cells; Intellectual Disabilityen
dc.titleHCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.en
dc.typeJournal articleen
dc.identifier.rmid0030024232en
dc.identifier.doi10.1093/hmg/ddv083en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/628952en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1041920en
dc.identifier.pubid176339-
pubs.library.collectionPaediatrics publicationsen
pubs.library.teamDS12en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidJolly, L. [0000-0003-4538-2658]en
dc.identifier.orcidBarry, S. [0000-0002-0597-7609]en
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Paediatrics publications

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