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A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations

Basement membranes (BMs) are ubiquitous extracellular matrices whose composition remains elusive, limiting our understanding of BM regulation and function. By developing a bioinformatic and in vivo discovery pipeline, we define a network of 222 human proteins and their animal orthologs localized to...

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Detalles Bibliográficos
Autores principales: Jayadev, Ranjay, Morais, Mychel R. P. T., Ellingford, Jamie M., Srinivasan, Sandhya, Naylor, Richard W., Lawless, Craig, Li, Anna S., Ingham, Jack F., Hastie, Eric, Chi, Qiuyi, Fresquet, Maryline, Koudis, Nikki-Maria, Thomas, Huw B., O’Keefe, Raymond T., Williams, Emily, Adamson, Antony, Stuart, Helen M., Banka, Siddharth, Smedley, Damian, Sherwood, David R., Lennon, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116610/
https://www.ncbi.nlm.nih.gov/pubmed/35584218
http://dx.doi.org/10.1126/sciadv.abn2265
Descripción
Sumario:Basement membranes (BMs) are ubiquitous extracellular matrices whose composition remains elusive, limiting our understanding of BM regulation and function. By developing a bioinformatic and in vivo discovery pipeline, we define a network of 222 human proteins and their animal orthologs localized to BMs. Network analysis and screening in C. elegans and zebrafish uncovered BM regulators, including ADAMTS, ROBO, and TGFβ. More than 100 BM network genes associate with human phenotypes, and by screening 63,039 genomes from families with rare disorders, we found loss-of-function variants in LAMA5, MPZL2, and MATN2 and show that they regulate BM composition and function. This cross-disciplinary study establishes the immense complexity of BMs and their impact on in human health.