Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.
Identifieur interne : 002774 ( Ncbi/Checkpoint ); précédent : 002773; suivant : 002775Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.
Auteurs : Chuan Tan ; Chloe Shard ; Enzo Ranieri [Australie] ; Kim Hynes ; Duyen H. Pham [Australie] ; Damian Leach [Australie] ; Grant Buchanan [Australie] ; Mark Corbett ; Cheryl Shoubridge [Australie] ; Raman Kumar [Australie] ; Evelyn Douglas [Australie] ; Lam S. Nguyen [France] ; Jacinta Mcmahon [Australie] ; Lynette Sadleir [Nouvelle-Zélande] ; Nicola Specchio [Italie] ; Carla Marini [Italie] ; Renzo Guerrini [Italie] ; Rikke S. Moller [Danemark] ; Christel Depienne [France] ; Eric Haan [Australie] ; Paul Q. Thomas ; Samuel F. Berkovic [Australie] ; Ingrid E. Scheffer [Australie] ; Jozef Gecz [Australie]Source :
- Human molecular genetics [ 1460-2083 ] ; 2015.
Descripteurs français
- KwdFr :
- 3-Hydroxysteroid dehydrogenases (génétique), 3-Hydroxysteroid dehydrogenases (métabolisme), Adolescent, Adulte, Adulte d'âge moyen, Analyse de profil d'expression de gènes, Analyse de regroupements, Cadhérines (génétique), Déficience intellectuelle (génétique), Enfant, Enfant d'âge préscolaire, Femelle, Fibroblastes (métabolisme), Humains, Hydroxyprostaglandine dehydrogenases (génétique), Hydroxyprostaglandine dehydrogenases (métabolisme), Jeune adulte, Mutation, Nourrisson, Nouveau-né, Phénotype, Prégnanolone (déficit), Prégnanolone (sang), Reproductibilité des résultats, Régulation de l'expression des gènes, Réseaux de régulation génique, Transduction du signal, Âge de début, Épilepsie (diagnostic), Épilepsie (génétique), Épilepsie (sang).
- MESH :
- diagnostic : Épilepsie.
- déficit : Prégnanolone.
- génétique : 3-Hydroxysteroid dehydrogenases, Cadhérines, Déficience intellectuelle, Hydroxyprostaglandine dehydrogenases, Épilepsie.
- métabolisme : 3-Hydroxysteroid dehydrogenases, Fibroblastes, Hydroxyprostaglandine dehydrogenases.
- sang : Prégnanolone, Épilepsie.
- Adolescent, Adulte, Adulte d'âge moyen, Analyse de profil d'expression de gènes, Analyse de regroupements, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Jeune adulte, Mutation, Nourrisson, Nouveau-né, Phénotype, Reproductibilité des résultats, Régulation de l'expression des gènes, Réseaux de régulation génique, Transduction du signal, Âge de début.
English descriptors
- KwdEn :
- 3-Hydroxysteroid Dehydrogenases (genetics), 3-Hydroxysteroid Dehydrogenases (metabolism), Adolescent, Adult, Age of Onset, Cadherins (genetics), Child, Child, Preschool, Cluster Analysis, Epilepsy (blood), Epilepsy (diagnosis), Epilepsy (genetics), Female, Fibroblasts (metabolism), Gene Expression Profiling, Gene Expression Regulation, Gene Regulatory Networks, Humans, Hydroxyprostaglandin Dehydrogenases (genetics), Hydroxyprostaglandin Dehydrogenases (metabolism), Infant, Infant, Newborn, Intellectual Disability (genetics), Middle Aged, Mutation, Phenotype, Pregnanolone (blood), Pregnanolone (deficiency), Reproducibility of Results, Signal Transduction, Young Adult.
- MESH :
- chemical , blood : Pregnanolone.
- chemical , deficiency : Pregnanolone.
- chemical , genetics : 3-Hydroxysteroid Dehydrogenases, Cadherins, Hydroxyprostaglandin Dehydrogenases.
- chemical , metabolism : 3-Hydroxysteroid Dehydrogenases, Hydroxyprostaglandin Dehydrogenases.
- blood : Epilepsy.
- diagnosis : Epilepsy.
- genetics : Epilepsy, Intellectual Disability.
- metabolism : Fibroblasts.
- Adolescent, Adult, Age of Onset, Child, Child, Preschool, Cluster Analysis, Female, Gene Expression Profiling, Gene Expression Regulation, Gene Regulatory Networks, Humans, Infant, Infant, Newborn, Middle Aged, Mutation, Phenotype, Reproducibility of Results, Signal Transduction, Young Adult.
Abstract
Protocadherin 19 (PCDH19) female limited epilepsy (PCDH19-FE; also known as epilepsy and mental retardation limited to females, EFMR; MIM300088) is an infantile onset epilepsy syndrome with or without intellectual disability (ID) and autism. We investigated transcriptomes of PCDH19-FE female and control primary skin fibroblasts, which are endowed to metabolize neurosteroid hormones. We identified a set of 94 significantly dysregulated genes in PCDH19-FE females. Intriguingly, 43 of the 94 genes (45.7%) showed gender-biased expression; enrichment of such genes was highly significant (P = 2.51E-47, two-tailed Fisher exact test). We further investigated the AKR1C1-3 genes, which encode crucial steroid hormone-metabolizing enzymes whose key products include allopregnanolone and estradiol. Both mRNA and protein levels of AKR1C3 were significantly decreased in PCDH19-FE patients. In agreement with this, the blood levels of allopregnanolone were also (P < 0.01) reduced. In conclusion, we show that the deficiency of neurosteroid allopregnanolone, one of the most potent GABA receptor modulators, may contribute to PCDH19-FE. Overall our findings provide evidence for a role of neurosteroids in epilepsy, ID and autism and create realistic opportunities for targeted therapeutic interventions.
DOI: 10.1093/hmg/ddv245
PubMed: 26123493
Affiliations:
- Australie, Danemark, France, Italie, Nouvelle-Zélande
- Victoria (État), Île-de-France
- Melbourne, Paris
- Université de Melbourne
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pubmed:26123493Le document en format XML
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<author><name sortKey="Nguyen, Lam S" sort="Nguyen, Lam S" uniqKey="Nguyen L" first="Lam S" last="Nguyen">Lam S. Nguyen</name>
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<author><name sortKey="Specchio, Nicola" sort="Specchio, Nicola" uniqKey="Specchio N" first="Nicola" last="Specchio">Nicola Specchio</name>
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<author><name sortKey="Marini, Carla" sort="Marini, Carla" uniqKey="Marini C" first="Carla" last="Marini">Carla Marini</name>
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<author><name sortKey="Guerrini, Renzo" sort="Guerrini, Renzo" uniqKey="Guerrini R" first="Renzo" last="Guerrini">Renzo Guerrini</name>
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<author><name sortKey="Moller, Rikke S" sort="Moller, Rikke S" uniqKey="Moller R" first="Rikke S" last="Moller">Rikke S. Moller</name>
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<author><name sortKey="Depienne, Christel" sort="Depienne, Christel" uniqKey="Depienne C" first="Christel" last="Depienne">Christel Depienne</name>
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<author><name sortKey="Haan, Eric" sort="Haan, Eric" uniqKey="Haan E" first="Eric" last="Haan">Eric Haan</name>
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<author><name sortKey="Thomas, Paul Q" sort="Thomas, Paul Q" uniqKey="Thomas P" first="Paul Q" last="Thomas">Paul Q. Thomas</name>
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<author><name sortKey="Berkovic, Samuel F" sort="Berkovic, Samuel F" uniqKey="Berkovic S" first="Samuel F" last="Berkovic">Samuel F. Berkovic</name>
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<author><name sortKey="Scheffer, Ingrid E" sort="Scheffer, Ingrid E" uniqKey="Scheffer I" first="Ingrid E" last="Scheffer">Ingrid E. Scheffer</name>
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<country xml:lang="fr">Australie</country>
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<author><name sortKey="Gecz, Jozef" sort="Gecz, Jozef" uniqKey="Gecz J" first="Jozef" last="Gecz">Jozef Gecz</name>
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<country wicri:rule="url">Australie</country>
<wicri:regionArea>School of Paediatrics and Reproductive Health, School of Molecular and Biomedical Sciences, SA Pathology, Adelaide, Australia, Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia</wicri:regionArea>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.</title>
<author><name sortKey="Tan, Chuan" sort="Tan, Chuan" uniqKey="Tan C" first="Chuan" last="Tan">Chuan Tan</name>
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<author><name sortKey="Ranieri, Enzo" sort="Ranieri, Enzo" uniqKey="Ranieri E" first="Enzo" last="Ranieri">Enzo Ranieri</name>
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<author><name sortKey="Pham, Duyen H" sort="Pham, Duyen H" uniqKey="Pham D" first="Duyen H" last="Pham">Duyen H. Pham</name>
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<author><name sortKey="Leach, Damian" sort="Leach, Damian" uniqKey="Leach D" first="Damian" last="Leach">Damian Leach</name>
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<author><name sortKey="Buchanan, Grant" sort="Buchanan, Grant" uniqKey="Buchanan G" first="Grant" last="Buchanan">Grant Buchanan</name>
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<author><name sortKey="Corbett, Mark" sort="Corbett, Mark" uniqKey="Corbett M" first="Mark" last="Corbett">Mark Corbett</name>
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<author><name sortKey="Shoubridge, Cheryl" sort="Shoubridge, Cheryl" uniqKey="Shoubridge C" first="Cheryl" last="Shoubridge">Cheryl Shoubridge</name>
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<author><name sortKey="Kumar, Raman" sort="Kumar, Raman" uniqKey="Kumar R" first="Raman" last="Kumar">Raman Kumar</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Paediatrics and Reproductive Health, Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>School of Paediatrics and Reproductive Health, Robinson Research Institute, The University of Adelaide, Adelaide, SA</wicri:regionArea>
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</affiliation>
</author>
<author><name sortKey="Douglas, Evelyn" sort="Douglas, Evelyn" uniqKey="Douglas E" first="Evelyn" last="Douglas">Evelyn Douglas</name>
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<country xml:lang="fr">Australie</country>
<wicri:regionArea>SA Pathology, Adelaide</wicri:regionArea>
<wicri:noRegion>Adelaide</wicri:noRegion>
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<author><name sortKey="Nguyen, Lam S" sort="Nguyen, Lam S" uniqKey="Nguyen L" first="Lam S" last="Nguyen">Lam S. Nguyen</name>
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<wicri:noRegion>Wellington</wicri:noRegion>
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</author>
<author><name sortKey="Specchio, Nicola" sort="Specchio, Nicola" uniqKey="Specchio N" first="Nicola" last="Specchio">Nicola Specchio</name>
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<wicri:noRegion>P.za S. Onofrio Rome 400165</wicri:noRegion>
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<author><name sortKey="Marini, Carla" sort="Marini, Carla" uniqKey="Marini C" first="Carla" last="Marini">Carla Marini</name>
<affiliation wicri:level="1"><nlm:affiliation>Neuroscience Department, Children's Hospital A. Meyer, University of Florence, Firenze, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Neuroscience Department, Children's Hospital A. Meyer, University of Florence, Firenze</wicri:regionArea>
<wicri:noRegion>Firenze</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Guerrini, Renzo" sort="Guerrini, Renzo" uniqKey="Guerrini R" first="Renzo" last="Guerrini">Renzo Guerrini</name>
<affiliation wicri:level="1"><nlm:affiliation>Neuroscience Department, Children's Hospital A. Meyer, University of Florence, Firenze, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Neuroscience Department, Children's Hospital A. Meyer, University of Florence, Firenze</wicri:regionArea>
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</affiliation>
</author>
<author><name sortKey="Moller, Rikke S" sort="Moller, Rikke S" uniqKey="Moller R" first="Rikke S" last="Moller">Rikke S. Moller</name>
<affiliation wicri:level="1"><nlm:affiliation>Danish Epilepsy Centre, Dianalund, Denmark, Institute of Regional Health Services Research, University of Southern Denmark, Odense, Denmark.</nlm:affiliation>
<country xml:lang="fr">Danemark</country>
<wicri:regionArea>Danish Epilepsy Centre, Dianalund, Denmark, Institute of Regional Health Services Research, University of Southern Denmark, Odense</wicri:regionArea>
<wicri:noRegion>Odense</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Depienne, Christel" sort="Depienne, Christel" uniqKey="Depienne C" first="Christel" last="Depienne">Christel Depienne</name>
<affiliation wicri:level="1"><nlm:affiliation>Inserm, CNRS, UM 75, U 1127, UMR 7225, ICM, Sorbonne Universités, UPMC Univ Paris 06, Paris F-75013, France, Département de Génétique et de Cytogénétique, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris F-75013, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Inserm, CNRS, UM 75, U 1127, UMR 7225, ICM, Sorbonne Universités, UPMC Univ Paris 06, Paris F-75013, France, Département de Génétique et de Cytogénétique, AP-HP, Hôpital de la Pitié-Salpêtrière, Paris F-75013</wicri:regionArea>
<wicri:noRegion>75013</wicri:noRegion>
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<region type="région" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Haan, Eric" sort="Haan, Eric" uniqKey="Haan E" first="Eric" last="Haan">Eric Haan</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Paediatrics and Reproductive Health, Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia, South Australian Clinical Genetics Service, SA Pathology, North Adelaide, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>School of Paediatrics and Reproductive Health, Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia, South Australian Clinical Genetics Service, SA Pathology, North Adelaide</wicri:regionArea>
<wicri:noRegion>North Adelaide</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Thomas, Paul Q" sort="Thomas, Paul Q" uniqKey="Thomas P" first="Paul Q" last="Thomas">Paul Q. Thomas</name>
<affiliation><nlm:affiliation>School of Molecular and Biomedical Sciences.</nlm:affiliation>
<wicri:noCountry code="no comma">School of Molecular and Biomedical Sciences.</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Berkovic, Samuel F" sort="Berkovic, Samuel F" uniqKey="Berkovic S" first="Samuel F" last="Berkovic">Samuel F. Berkovic</name>
<affiliation wicri:level="4"><nlm:affiliation>Epilepsy Research Centre, The University of Melbourne, Melbourne, VIC, Australia, Epilepsy Research Centre, The University of Melbourne, Melbourne, Australia and Florey Institute of Neuroscience and Mental Health, Melbourne, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Epilepsy Research Centre, The University of Melbourne, Melbourne, VIC, Australia, Epilepsy Research Centre, The University of Melbourne, Melbourne, Australia and Florey Institute of Neuroscience and Mental Health, Melbourne</wicri:regionArea>
<placeName><settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
<settlement type="city">Melbourne</settlement>
</placeName>
<orgName type="university">Université de Melbourne</orgName>
</affiliation>
</author>
<author><name sortKey="Scheffer, Ingrid E" sort="Scheffer, Ingrid E" uniqKey="Scheffer I" first="Ingrid E" last="Scheffer">Ingrid E. Scheffer</name>
<affiliation wicri:level="4"><nlm:affiliation>Epilepsy Research Centre, The University of Melbourne, Melbourne, VIC, Australia, Epilepsy Research Centre, The University of Melbourne, Melbourne, Australia and Florey Institute of Neuroscience and Mental Health, Melbourne, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Epilepsy Research Centre, The University of Melbourne, Melbourne, VIC, Australia, Epilepsy Research Centre, The University of Melbourne, Melbourne, Australia and Florey Institute of Neuroscience and Mental Health, Melbourne</wicri:regionArea>
<placeName><settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
<settlement type="city">Melbourne</settlement>
</placeName>
<orgName type="university">Université de Melbourne</orgName>
</affiliation>
</author>
<author><name sortKey="Gecz, Jozef" sort="Gecz, Jozef" uniqKey="Gecz J" first="Jozef" last="Gecz">Jozef Gecz</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Paediatrics and Reproductive Health, School of Molecular and Biomedical Sciences, SA Pathology, Adelaide, Australia, Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia, jozef.gecz@adelaide.edu.au.</nlm:affiliation>
<country wicri:rule="url">Australie</country>
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<series><title level="j">Human molecular genetics</title>
<idno type="eISSN">1460-2083</idno>
<imprint><date when="2015" type="published">2015</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>3-Hydroxysteroid Dehydrogenases (genetics)</term>
<term>3-Hydroxysteroid Dehydrogenases (metabolism)</term>
<term>Adolescent</term>
<term>Adult</term>
<term>Age of Onset</term>
<term>Cadherins (genetics)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Cluster Analysis</term>
<term>Epilepsy (blood)</term>
<term>Epilepsy (diagnosis)</term>
<term>Epilepsy (genetics)</term>
<term>Female</term>
<term>Fibroblasts (metabolism)</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation</term>
<term>Gene Regulatory Networks</term>
<term>Humans</term>
<term>Hydroxyprostaglandin Dehydrogenases (genetics)</term>
<term>Hydroxyprostaglandin Dehydrogenases (metabolism)</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Intellectual Disability (genetics)</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Phenotype</term>
<term>Pregnanolone (blood)</term>
<term>Pregnanolone (deficiency)</term>
<term>Reproducibility of Results</term>
<term>Signal Transduction</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>3-Hydroxysteroid dehydrogenases (génétique)</term>
<term>3-Hydroxysteroid dehydrogenases (métabolisme)</term>
<term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Analyse de profil d'expression de gènes</term>
<term>Analyse de regroupements</term>
<term>Cadhérines (génétique)</term>
<term>Déficience intellectuelle (génétique)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Fibroblastes (métabolisme)</term>
<term>Humains</term>
<term>Hydroxyprostaglandine dehydrogenases (génétique)</term>
<term>Hydroxyprostaglandine dehydrogenases (métabolisme)</term>
<term>Jeune adulte</term>
<term>Mutation</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Phénotype</term>
<term>Prégnanolone (déficit)</term>
<term>Prégnanolone (sang)</term>
<term>Reproductibilité des résultats</term>
<term>Régulation de l'expression des gènes</term>
<term>Réseaux de régulation génique</term>
<term>Transduction du signal</term>
<term>Âge de début</term>
<term>Épilepsie (diagnostic)</term>
<term>Épilepsie (génétique)</term>
<term>Épilepsie (sang)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Pregnanolone</term>
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<keywords scheme="MESH" type="chemical" qualifier="deficiency" xml:lang="en"><term>Pregnanolone</term>
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<term>Cadherins</term>
<term>Hydroxyprostaglandin Dehydrogenases</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>3-Hydroxysteroid Dehydrogenases</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Epilepsy</term>
<term>Intellectual Disability</term>
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<term>Cadhérines</term>
<term>Déficience intellectuelle</term>
<term>Hydroxyprostaglandine dehydrogenases</term>
<term>Épilepsie</term>
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</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>3-Hydroxysteroid dehydrogenases</term>
<term>Fibroblastes</term>
<term>Hydroxyprostaglandine dehydrogenases</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Prégnanolone</term>
<term>Épilepsie</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age of Onset</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Cluster Analysis</term>
<term>Female</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation</term>
<term>Gene Regulatory Networks</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Phenotype</term>
<term>Reproducibility of Results</term>
<term>Signal Transduction</term>
<term>Young Adult</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Analyse de profil d'expression de gènes</term>
<term>Analyse de regroupements</term>
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<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
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<term>Jeune adulte</term>
<term>Mutation</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Phénotype</term>
<term>Reproductibilité des résultats</term>
<term>Régulation de l'expression des gènes</term>
<term>Réseaux de régulation génique</term>
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<front><div type="abstract" xml:lang="en">Protocadherin 19 (PCDH19) female limited epilepsy (PCDH19-FE; also known as epilepsy and mental retardation limited to females, EFMR; MIM300088) is an infantile onset epilepsy syndrome with or without intellectual disability (ID) and autism. We investigated transcriptomes of PCDH19-FE female and control primary skin fibroblasts, which are endowed to metabolize neurosteroid hormones. We identified a set of 94 significantly dysregulated genes in PCDH19-FE females. Intriguingly, 43 of the 94 genes (45.7%) showed gender-biased expression; enrichment of such genes was highly significant (P = 2.51E-47, two-tailed Fisher exact test). We further investigated the AKR1C1-3 genes, which encode crucial steroid hormone-metabolizing enzymes whose key products include allopregnanolone and estradiol. Both mRNA and protein levels of AKR1C3 were significantly decreased in PCDH19-FE patients. In agreement with this, the blood levels of allopregnanolone were also (P < 0.01) reduced. In conclusion, we show that the deficiency of neurosteroid allopregnanolone, one of the most potent GABA receptor modulators, may contribute to PCDH19-FE. Overall our findings provide evidence for a role of neurosteroids in epilepsy, ID and autism and create realistic opportunities for targeted therapeutic interventions.</div>
</front>
</TEI>
<affiliations><list><country><li>Australie</li>
<li>Danemark</li>
<li>France</li>
<li>Italie</li>
<li>Nouvelle-Zélande</li>
</country>
<region><li>Victoria (État)</li>
<li>Île-de-France</li>
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<settlement><li>Melbourne</li>
<li>Paris</li>
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<orgName><li>Université de Melbourne</li>
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<name sortKey="Shard, Chloe" sort="Shard, Chloe" uniqKey="Shard C" first="Chloe" last="Shard">Chloe Shard</name>
<name sortKey="Tan, Chuan" sort="Tan, Chuan" uniqKey="Tan C" first="Chuan" last="Tan">Chuan Tan</name>
<name sortKey="Thomas, Paul Q" sort="Thomas, Paul Q" uniqKey="Thomas P" first="Paul Q" last="Thomas">Paul Q. Thomas</name>
</noCountry>
<country name="Australie"><noRegion><name sortKey="Ranieri, Enzo" sort="Ranieri, Enzo" uniqKey="Ranieri E" first="Enzo" last="Ranieri">Enzo Ranieri</name>
</noRegion>
<name sortKey="Berkovic, Samuel F" sort="Berkovic, Samuel F" uniqKey="Berkovic S" first="Samuel F" last="Berkovic">Samuel F. Berkovic</name>
<name sortKey="Buchanan, Grant" sort="Buchanan, Grant" uniqKey="Buchanan G" first="Grant" last="Buchanan">Grant Buchanan</name>
<name sortKey="Douglas, Evelyn" sort="Douglas, Evelyn" uniqKey="Douglas E" first="Evelyn" last="Douglas">Evelyn Douglas</name>
<name sortKey="Gecz, Jozef" sort="Gecz, Jozef" uniqKey="Gecz J" first="Jozef" last="Gecz">Jozef Gecz</name>
<name sortKey="Haan, Eric" sort="Haan, Eric" uniqKey="Haan E" first="Eric" last="Haan">Eric Haan</name>
<name sortKey="Kumar, Raman" sort="Kumar, Raman" uniqKey="Kumar R" first="Raman" last="Kumar">Raman Kumar</name>
<name sortKey="Leach, Damian" sort="Leach, Damian" uniqKey="Leach D" first="Damian" last="Leach">Damian Leach</name>
<name sortKey="Mcmahon, Jacinta" sort="Mcmahon, Jacinta" uniqKey="Mcmahon J" first="Jacinta" last="Mcmahon">Jacinta Mcmahon</name>
<name sortKey="Pham, Duyen H" sort="Pham, Duyen H" uniqKey="Pham D" first="Duyen H" last="Pham">Duyen H. Pham</name>
<name sortKey="Scheffer, Ingrid E" sort="Scheffer, Ingrid E" uniqKey="Scheffer I" first="Ingrid E" last="Scheffer">Ingrid E. Scheffer</name>
<name sortKey="Shoubridge, Cheryl" sort="Shoubridge, Cheryl" uniqKey="Shoubridge C" first="Cheryl" last="Shoubridge">Cheryl Shoubridge</name>
</country>
<country name="France"><region name="Île-de-France"><name sortKey="Nguyen, Lam S" sort="Nguyen, Lam S" uniqKey="Nguyen L" first="Lam S" last="Nguyen">Lam S. Nguyen</name>
</region>
<name sortKey="Depienne, Christel" sort="Depienne, Christel" uniqKey="Depienne C" first="Christel" last="Depienne">Christel Depienne</name>
</country>
<country name="Nouvelle-Zélande"><noRegion><name sortKey="Sadleir, Lynette" sort="Sadleir, Lynette" uniqKey="Sadleir L" first="Lynette" last="Sadleir">Lynette Sadleir</name>
</noRegion>
</country>
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</country>
<country name="Danemark"><noRegion><name sortKey="Moller, Rikke S" sort="Moller, Rikke S" uniqKey="Moller R" first="Rikke S" last="Moller">Rikke S. Moller</name>
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