Publication Date
5-17-2025
Journal
Human Molecular Genetics
DOI
10.1093/hmg/ddaf050
PMID
40237576
PMCID
PMC12085778
PubMedCentral® Posted Date
4-16-2025
PubMedCentral® Full Text Version
Post-print
Abstract
Laminin B1 (LAMB1) is one of the extracellular matrix (ECM) proteins that make up the basement membrane. Early frameshift, late frameshift, and missense variants in LAMB1 have been reported to cause rare monogenic neurological disorders that are collectively known as LAMB1-related leukoencephalopathy. Although there is some genotype-phenotype correlation, functional consequences of pathogenic LAMB1 variants are largely unknown. In this study, we aimed to elucidate function of the fly ortholog of this gene (LanB1) in the nervous system and to further study the functional consequences of the LAMB1 variants using Drosophila melanogaster. We found that the LanB1 gene is expressed on the surface of adult fly brains in a subset of glia cells. We further found that LanB1 protein localizes to the blood-brain barrier (BBB) in adult fly brains and knockdown of LanB1 in the BBB resulted in short life span and locomotor defects. Although human LAMB1 was not able to function in flies, in vivo overexpression and rescue experiments using analogous variants in fly LanB1 suggested that the frameshift variants behave as strong loss-of-function (LoF) alleles whereas a missense variant functions as a milder LoF allele. In vitro assay in HEK293T cells revealed that late-truncated LAMB1 is uniquely detected as a monomer in the culture medium, which might be the basis of dominant inheritance of these variants through a gain-of-function mechanism. Our data contributes to the understanding of the ECM component of the fly BBB and lays the foundation to unravel the molecular consequences of different pathogenic variants in LAMB1.
Keywords
Animals, Humans, Drosophila melanogaster, Leukoencephalopathies, Neuroglia, Laminin, Genetic Association Studies, Blood-Brain Barrier, Drosophila Proteins, Brain, Frameshift Mutation, Mutation, Missense, Phenotype, Disease Models, Animal, LAMB1, LanB1, leukoencephalopathy, Drosophila, blood-brain barrier
Published Open-Access
yes
Recommended Citation
Yasuda, Rei; Hashimoto, Hirokazu; Oka, Mikiko; et al., "Functional Analysis of Pathogenic Variants in LAMB1-Related Leukoencephalopathy Reveals Genotype-Phenotype Correlations and Suggests Its Role in Glial Cells" (2025). Faculty, Staff and Students Publications. 7180.
https://digitalcommons.library.tmc.edu/baylor_docs/7180