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Development of a Quantitative FMRP Assay for Mouse Tissue Applications

Fragile X syndrome results from the absence of the FMR1 gene product—Fragile X Mental Retardation Protein (FMRP). Fragile X animal research has lacked a reliable method to quantify FMRP. We report the development of an array of FMRP-specific monoclonal antibodies and their application for quantitati...

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Autores principales: Adayev, Tatyana, LaFauci, Giuseppe, Xu, Weimin, Dobkin, Carl, Kascsak, Richard, Brown, W. Ted, Goodman, Jeffrey H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535242/
https://www.ncbi.nlm.nih.gov/pubmed/34680911
http://dx.doi.org/10.3390/genes12101516
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author Adayev, Tatyana
LaFauci, Giuseppe
Xu, Weimin
Dobkin, Carl
Kascsak, Richard
Brown, W. Ted
Goodman, Jeffrey H.
author_facet Adayev, Tatyana
LaFauci, Giuseppe
Xu, Weimin
Dobkin, Carl
Kascsak, Richard
Brown, W. Ted
Goodman, Jeffrey H.
author_sort Adayev, Tatyana
collection PubMed
description Fragile X syndrome results from the absence of the FMR1 gene product—Fragile X Mental Retardation Protein (FMRP). Fragile X animal research has lacked a reliable method to quantify FMRP. We report the development of an array of FMRP-specific monoclonal antibodies and their application for quantitative assessment of FMRP (qFMRPm) in mouse tissue. To characterize the assay, we determined the normal variability of FMRP expression in four brain structures of six different mouse strains at seven weeks of age. There was a hierarchy of FMRP expression: neocortex > hippocampus > cerebellum > brainstem. The expression of FMRP was highest and least variable in the neocortex, whereas it was most variable in the hippocampus. Male C57Bl/6J and FVB mice were selected to determine FMRP developmental differences in the brain at 3, 7, 10, and 14 weeks of age. We examined the four structures and found a developmental decline in FMRP expression with age, except for the brainstem where it remained stable. qFMRPm assay of blood had highest values in 3 week old animals and dropped by 2.5-fold with age. Sex differences were not significant. The results establish qFMRPm as a valuable tool due to its ease of methodology, cost effectiveness, and accuracy.
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spelling pubmed-85352422021-10-23 Development of a Quantitative FMRP Assay for Mouse Tissue Applications Adayev, Tatyana LaFauci, Giuseppe Xu, Weimin Dobkin, Carl Kascsak, Richard Brown, W. Ted Goodman, Jeffrey H. Genes (Basel) Article Fragile X syndrome results from the absence of the FMR1 gene product—Fragile X Mental Retardation Protein (FMRP). Fragile X animal research has lacked a reliable method to quantify FMRP. We report the development of an array of FMRP-specific monoclonal antibodies and their application for quantitative assessment of FMRP (qFMRPm) in mouse tissue. To characterize the assay, we determined the normal variability of FMRP expression in four brain structures of six different mouse strains at seven weeks of age. There was a hierarchy of FMRP expression: neocortex > hippocampus > cerebellum > brainstem. The expression of FMRP was highest and least variable in the neocortex, whereas it was most variable in the hippocampus. Male C57Bl/6J and FVB mice were selected to determine FMRP developmental differences in the brain at 3, 7, 10, and 14 weeks of age. We examined the four structures and found a developmental decline in FMRP expression with age, except for the brainstem where it remained stable. qFMRPm assay of blood had highest values in 3 week old animals and dropped by 2.5-fold with age. Sex differences were not significant. The results establish qFMRPm as a valuable tool due to its ease of methodology, cost effectiveness, and accuracy. MDPI 2021-09-26 /pmc/articles/PMC8535242/ /pubmed/34680911 http://dx.doi.org/10.3390/genes12101516 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Adayev, Tatyana
LaFauci, Giuseppe
Xu, Weimin
Dobkin, Carl
Kascsak, Richard
Brown, W. Ted
Goodman, Jeffrey H.
Development of a Quantitative FMRP Assay for Mouse Tissue Applications
title Development of a Quantitative FMRP Assay for Mouse Tissue Applications
title_full Development of a Quantitative FMRP Assay for Mouse Tissue Applications
title_fullStr Development of a Quantitative FMRP Assay for Mouse Tissue Applications
title_full_unstemmed Development of a Quantitative FMRP Assay for Mouse Tissue Applications
title_short Development of a Quantitative FMRP Assay for Mouse Tissue Applications
title_sort development of a quantitative fmrp assay for mouse tissue applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535242/
https://www.ncbi.nlm.nih.gov/pubmed/34680911
http://dx.doi.org/10.3390/genes12101516
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