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Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking

Authors :
Sanderson, Leslie E.
Lanko, Kristina
Alsagob, Maysoon
Almass, Rawan
Al-Ahmadi, Nada
Najafi, Maryam
Al-Muhaizea, Mohammad A.
Alzaidan, Hamad
Aldhalaan, Hesham
Perenthaler, Elena
Van Der Linde, Herma C.
Nikoncuk, Anita
Kühn, Nikolas A.
Antony, Dinu
Owaidah, Tarek Mustafa
Raskin, Salmo
Vieira, Luana Gabriela Dalla Rosa
Mombach, Romulo
Ahangari, Najmeh
Silveira, Tainá Regina Damaceno
Ameziane, Najim
Rolfs, Arndt
Alharbi, Aljohara
Sabbagh, Raghda M.
Alahmadi, Khalid
Alawam, Bashayer
Ghebeh, Hazem
Alhargan, Aljouhra
Albader, Anoud A.
Binhumaid, Faisal S.
Goljan, Ewa
Monies, Dorota
Mustafa, Osama M.
Aldosary, Mazhor
Albakheet, Albandary
Alyounes, Banan
Almutairi, Faten
Al-Odaib, Ali
Aksoy, Durdane Bekar
Basak, A. Nazli
Palvadeau, Robin
Trabzuni, Daniah
Rosenfeld, Jill A.
Karimiani, Ehsan Ghayoor
Meyer, Brian F.
Karakas, Bedri
Al-Mohanna, Futwan
Arold, Stefan T.
Colak, Dilek
Maroofian, Reza
Houlden, Henry
Bertoli-Avella, Aida M.
Schmidts, Miriam
Barakat, Tahsin Stefan
Van Ham, Tjakko J.
Kaya, Namik
Sanderson, Leslie E.
Lanko, Kristina
Alsagob, Maysoon
Almass, Rawan
Al-Ahmadi, Nada
Najafi, Maryam
Al-Muhaizea, Mohammad A.
Alzaidan, Hamad
Aldhalaan, Hesham
Perenthaler, Elena
Van Der Linde, Herma C.
Nikoncuk, Anita
Kühn, Nikolas A.
Antony, Dinu
Owaidah, Tarek Mustafa
Raskin, Salmo
Vieira, Luana Gabriela Dalla Rosa
Mombach, Romulo
Ahangari, Najmeh
Silveira, Tainá Regina Damaceno
Ameziane, Najim
Rolfs, Arndt
Alharbi, Aljohara
Sabbagh, Raghda M.
Alahmadi, Khalid
Alawam, Bashayer
Ghebeh, Hazem
Alhargan, Aljouhra
Albader, Anoud A.
Binhumaid, Faisal S.
Goljan, Ewa
Monies, Dorota
Mustafa, Osama M.
Aldosary, Mazhor
Albakheet, Albandary
Alyounes, Banan
Almutairi, Faten
Al-Odaib, Ali
Aksoy, Durdane Bekar
Basak, A. Nazli
Palvadeau, Robin
Trabzuni, Daniah
Rosenfeld, Jill A.
Karimiani, Ehsan Ghayoor
Meyer, Brian F.
Karakas, Bedri
Al-Mohanna, Futwan
Arold, Stefan T.
Colak, Dilek
Maroofian, Reza
Houlden, Henry
Bertoli-Avella, Aida M.
Schmidts, Miriam
Barakat, Tahsin Stefan
Van Ham, Tjakko J.
Kaya, Namik
Source :
Sanderson , L E , Lanko , K , Alsagob , M , Almass , R , Al-Ahmadi , N , Najafi , M , Al-Muhaizea , M A , Alzaidan , H , Aldhalaan , H , Perenthaler , E , Van Der Linde , H C , Nikoncuk , A , Kühn , N A , Antony , D , Owaidah , T M , Raskin , S , Vieira , L G D R , Mombach , R , Ahangari , N , Silveira , T R D , Ameziane , N , Rolfs , A , Alharbi , A , Sabbagh , R M , Alahmadi , K , Alawam , B , Ghebeh , H , Alhargan , A , Albader , A A , Binhumaid , F S , Goljan , E , Monies , D , Mustafa , O M , Aldosary , M , Albakheet , A , Alyounes , B , Almutairi , F , Al-Odaib , A , Aksoy , D B , Basak , A N , Palvadeau , R , Trabzuni , D , Rosenfeld , J A , Karimiani , E G , Meyer , B F , Karakas , B , Al-Mohanna , F , Arold , S T , Colak , D , Maroofian , R , Houlden , H , Bertoli-Avella , A M , Schmidts , M , Barakat , T S , Van Ham , T J & Kaya , N 2021 , ' Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking ' , Brain , vol. 144 , no. 3 , pp. 769-780 .
Publication Year :
2021

Abstract

Membrane trafficking is a complex, essential process in eukaryotic cells responsible for protein transport and processing. Deficiencies in vacuolar protein sorting (VPS) proteins, key regulators of trafficking, cause abnormal intracellular segregation of macromolecules and organelles and are linked to human disease. VPS proteins function as part of complexes such as the homotypic fusion and vacuole protein sorting (HOPS) tethering complex, composed of VPS11, VPS16, VPS18, VPS33A, VPS39 and VPS41. The HOPS-specific subunit VPS41 has been reported to promote viability of dopaminergic neurons in Parkinson's disease but to date has not been linked to human disease. Here, we describe five unrelated families with nine affected individuals, all carrying homozygous variants in VPS41 that we show impact protein function. All affected individuals presented with a progressive neurodevelopmental disorder consisting of cognitive impairment, cerebellar atrophy/hypoplasia, motor dysfunction with ataxia and dystonia, and nystagmus. Zebrafish disease modelling supports the involvement of VPS41 dysfunction in the disorder, indicating lysosomal dysregulation throughout the brain and providing support for cerebellar and microglial abnormalities when vps41 was mutated. This provides the first example of human disease linked to the HOPS-specific subunit VPS41 and suggests the importance of HOPS complex activity for cerebellar function.

Details

Database :
OAIster
Journal :
Sanderson , L E , Lanko , K , Alsagob , M , Almass , R , Al-Ahmadi , N , Najafi , M , Al-Muhaizea , M A , Alzaidan , H , Aldhalaan , H , Perenthaler , E , Van Der Linde , H C , Nikoncuk , A , Kühn , N A , Antony , D , Owaidah , T M , Raskin , S , Vieira , L G D R , Mombach , R , Ahangari , N , Silveira , T R D , Ameziane , N , Rolfs , A , Alharbi , A , Sabbagh , R M , Alahmadi , K , Alawam , B , Ghebeh , H , Alhargan , A , Albader , A A , Binhumaid , F S , Goljan , E , Monies , D , Mustafa , O M , Aldosary , M , Albakheet , A , Alyounes , B , Almutairi , F , Al-Odaib , A , Aksoy , D B , Basak , A N , Palvadeau , R , Trabzuni , D , Rosenfeld , J A , Karimiani , E G , Meyer , B F , Karakas , B , Al-Mohanna , F , Arold , S T , Colak , D , Maroofian , R , Houlden , H , Bertoli-Avella , A M , Schmidts , M , Barakat , T S , Van Ham , T J & Kaya , N 2021 , ' Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking ' , Brain , vol. 144 , no. 3 , pp. 769-780 .
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1322185188
Document Type :
Electronic Resource