4.7 Article

Evaluation of UBE3A antibodies in mice and human cerebral organoids

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41598-021-85923-x

Keywords

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Funding

  1. Simons Foundation SFARI Explorers Grant [495112]
  2. NCSU Faculty Research and Professional Development Program
  3. NCSU Research Innovation Seed Fund Grant
  4. NSF Emerging Frontiers in Research and Innovation program [NSF-1830910]
  5. NIH Avenir Award [DP1-DA044359]
  6. Foundation for Angelman Syndrome Therapeutics Targeted Research to Advance a Cure Grant [FT2020-003]
  7. American Association of University Women

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This study evaluated the specificities of seven commercial UBE3A antibodies and found that three of them showed substantial nonspecific immunoreactivity. While four antibodies demonstrated specific localization patterns in both mouse brain sections and human cerebral organoids, they varied significantly in background signals and staining patterns in undifferentiated human pluripotent stem cells.
UBE3A is an E3 ubiquitin ligase encoded by the neurally imprinted UBE3A gene. The abundance and subcellular distribution of UBE3A has been the topic of many previous studies as its dosage and localization has been linked to neurodevelopmental disorders including Autism, Dup15q syndrome, and Angelman syndrome. While commercially available antibodies have been widely employed to determine UBE3A localization, an extensive analysis and comparison of the performance of different UBE3A antibodies has not been conducted. Here we evaluated the specificities of seven commercial UBE3A antibodies in two of the major experimental models used in UBE3A research, mouse and human pluripotent stem cell-derived neural cells and tissues. We tested these antibodies in their two most common assays, immunofluorescence and western blot. In addition, we also assessed the ability of these antibodies to capture dynamic spatiotemporal changes of UBE3A by utilizing human cerebral organoid models. Our results reveal that among the seven antibodies tested, three antibodies demonstrated substantial nonspecific immunoreactivity. While four antibodies show specific localization patterns in both mouse brain sections and human cerebral organoids, these antibodies varied significantly in background signals and staining patterns in undifferentiated human pluripotent stem cells.

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