👤 Susan M Hiatt

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Jordy Dekker, Rachel Schot, Kimberly A Aldinger +87 more · 2025 · American journal of human genetics · Elsevier · added 2026-04-24
Jordy Dekker, Rachel Schot, Kimberly A Aldinger, David B Everman, Camerun Washington, Julie R Jones, Jennifer A Sullivan, Rebecca C Spillmann, Vandana Shashi, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Anne-Laure Mosca-Boidron, Laurence Perrin, Stéphane Auvin, Maha S Zaki, Joseph G Gleeson, Naomi Meave, Cassidy Wallace, Sophie Nambot, Julian Delanne, Sarah M Ruggiero, Ingo Helbig, Mark P Fitzgerald, Richard J Leventer, Dorothy K Grange, Emanuela Argilli, Elliott H Sherr, Supraja Prakash, Derek E Neilson, Francesco Nicita, Antonella Sferra, Enrico S Bertini, Chiara Aiello, Knut Brockmann, Alexander B Kuranov, Silke Kaulfuss, Sulman Basit, Majed Alluqmani, Ahmad Almatrafi, Jan M Friedman, Colleen Guimond, Faruq Mohammed, Pooja Sharma, Divya Goel, Thomas Wirth, Mathieu Anheim, Paulina Bahena, Asuman Koparir, Konstantinos Kolokotronis, Barbara Vona, Thomas Haaf, Erdmute Kunstmann, Reza Maroofian, Henrike L Sczakiel, Felix Boschann, Mala Misra-Isrie, Raymond J Louie, Elliot S Stolerman, Pedro A Sanchez-Lara, Sandra Mergler, Renske Oegema, Yuri A Zarate, Ariana Kariminejad, Homa Tajsharghi, Shimriet Zeidler, Anneke J A Kievit, Arjan Bouman, Gerarda Cappuccio, Nicola Brunetti-Pierri, Kyra E Stuurman, Dayna Morel Swols, Mustafa Tekin, Jariya Upadia, Donna M Martin, Daniel Craven, Susan M Hiatt, Laura A van de Pol, Felice D'Arco, Henri Margot, Martina Wilke, Soheil Yousefi, Tahsin Stefan Barakat, Monique M van Veghel-Plandsoen, Eleonora Aronica, Jasper Anink, Stephen L Rogers, Kevin C Slep, Dan Doherty, William B Dobyns, Grazia M S Mancini Show less
Microtubule-actin cross-linking factor 1 (MACF1) is a large protein of the spectraplakin family, which is essential for brain development. MACF1 interacts with microtubules through the growth arrest-s Show more
Microtubule-actin cross-linking factor 1 (MACF1) is a large protein of the spectraplakin family, which is essential for brain development. MACF1 interacts with microtubules through the growth arrest-specific 2 (Gas2)-related (GAR) domain. Heterozygous MACF1 missense variants affecting the zinc-binding residues in this domain result in a distinctive cortical and brain stem malformation. Evidence for other MACF1-associated disorders is still limited. Here, we present a cohort of 45 individuals with heterozygous or bi-allelic MACF1 variants to explore the phenotypic spectrum and assess possible pathogenic relevance. We observe that de novo heterozygous missense variants in the EF-hand domains also result in distinctive brain malformation and provide experimental evidence that variants in the EF-hand/GAR module increase microtubule binding, suggestive of a toxic gain of function. Notably, no phenotype-genotype correlation was possible for the remaining heterozygous variants in other domains. A clinical review of eight families with bi-allelic variants reveals a possible complex neurodevelopmental syndrome of the central and peripheral nervous systems. In these individuals, bi-allelic variants mostly affect the Plakin domain. Furthermore, RNA sequencing and chromatin immunoprecipitation (ChIP) analyses of human fetal brain tissue reveal five MACF1 isoforms with region-specific expression, differing in their exon 1 transcription start sites but splicing to a common exon 2. This differential expression explains the frontal-predominant lissencephaly in an individual with a homozygous stop-gain in exon 1 (MACF1-204: c.70C>T [p.Arg24∗]), as this isoform is preferentially expressed in the frontal cortex. We conclude that MACF1-related disorders are strictly linked to domain function and the level of transcript expression, explaining the observed wide clinical heterogeneity. Show less
no PDF DOI: 10.1016/j.ajhg.2025.08.010
MACF1
Ratna Tripathy, Ines Leca, Tessa van Dijk +38 more · 2018 · Neuron · Elsevier · added 2026-04-24
Corpus callosum malformations are associated with a broad range of neurodevelopmental diseases. We report that de novo mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia Show more
Corpus callosum malformations are associated with a broad range of neurodevelopmental diseases. We report that de novo mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations (MCC-CH-CM) in the absence of megalencephaly. We show that MAST1 is a microtubule-associated protein that is predominantly expressed in post-mitotic neurons and is present in both dendritic and axonal compartments. We further show that Mast1 null animals are phenotypically normal, whereas the deletion of a single amino acid (L278del) recapitulates the distinct neurological phenotype observed in patients. In animals harboring Mast1 microdeletions, we find that the PI3K/AKT3/mTOR pathway is unperturbed, whereas Mast2 and Mast3 levels are diminished, indicative of a dominant-negative mode of action. Finally, we report that de novo MAST1 substitutions are present in patients with autism and microcephaly, raising the prospect that mutations in this gene give rise to a spectrum of neurodevelopmental diseases. Show less
📄 PDF DOI: 10.1016/j.neuron.2018.10.044
MAST3