Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1784587732601798656 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8535242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT adayevtatyana developmentofaquantitativefmrpassayformousetissueapplications AT lafaucigiuseppe developmentofaquantitativefmrpassayformousetissueapplications AT xuweimin developmentofaquantitativefmrpassayformousetissueapplications AT dobkincarl developmentofaquantitativefmrpassayformousetissueapplications AT kascsakrichard developmentofaquantitativefmrpassayformousetissueapplications AT brownwted developmentofaquantitativefmrpassayformousetissueapplications AT goodmanjeffreyh developmentofaquantitativefmrpassayformousetissueapplications |