scholarly journals Development of a Quantitative FMRP Assay for Mouse Tissue Applications

Genes ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 1516
Author(s):  
Tatyana Adayev ◽  
Giuseppe LaFauci ◽  
Weimin Xu ◽  
Carl Dobkin ◽  
Richard Kascsak ◽  
...  

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.

2020 ◽  
Vol 12 (4) ◽  
pp. 903-916 ◽  
Author(s):  
Cassandra Malecki ◽  
Brett D. Hambly ◽  
Richmond W. Jeremy ◽  
Elizabeth N. Robertson

2005 ◽  
Vol 280 (39) ◽  
pp. 33403-33410 ◽  
Author(s):  
Francesca Zalfa ◽  
Salvatore Adinolfi ◽  
Ilaria Napoli ◽  
Eva Kühn-Hölsken ◽  
Henning Urlaub ◽  
...  

2005 ◽  
Vol 15 (12) ◽  
pp. 1156-1163 ◽  
Author(s):  
Simon P. Reeve ◽  
Laura Bassetto ◽  
Ginka K. Genova ◽  
Yelena Kleyner ◽  
Maarten Leyssen ◽  
...  

Author(s):  
Claudia Bagni ◽  
Eric Klann

Chapter 8 discusses how Fragile X syndrome (FXS) is caused by the absence of the RNA-binding protein fragile X mental retardation protein (FMRP). FMRP is highly expressed in the brain and gonads, the two organs mainly affected in patients with the syndrome. Functionally, FMRP belongs to the family of RNA-binding proteins, shuttling from the nucleus to the cytoplasm, and, as shown for other RNA-binding proteins, forms large messenger ribonucleoparticles.


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