Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets

F Zhang, Y Kang, M Wang, Y Li, T Xu…�- Human molecular�…, 2018 - academic.oup.com
Abstract N 6-methyladenosine (m6A) is the most prevalent internal modification of
mammalian messenger RNAs (mRNAs) and long non-coding RNAs. The biological�…

[HTML][HTML] The RNA-binding protein FMRP facilitates the nuclear export of N6-methyladenosine–containing mRNAs

PJ Hsu, H Shi, AC Zhu, Z Lu, N Miller, BM Edens…�- Journal of Biological�…, 2019 - ASBMB
N 6-Methyladenosine (m 6 A) is the most abundant post-transcriptional mRNA modification
in eukaryotes and exerts many of its effects on gene expression through reader proteins that�…

[HTML][HTML] FMRP modulates neural differentiation through m6A-dependent mRNA nuclear export

BM Edens, C Vissers, J Su, S Arumugam, Z Xu, H Shi…�- Cell reports, 2019 - cell.com
Summary N 6-methyladenosine (m 6 A) modification of mRNA is emerging as a vital
mechanism regulating RNA function. Here, we show that fragile X mental retardation protein�…

The molecular biology of FMRP: new insights into fragile X syndrome

JD Richter, X Zhao�- Nature Reviews Neuroscience, 2021 - nature.com
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation
1 gene (FMR1), a gene that—when epigenetically inactivated by a triplet nucleotide repeat�…

[HTML][HTML] The FMRP regulon: from targets to disease convergence

E Fern�ndez, N Rajan, C Bagni�- Frontiers in neuroscience, 2013 - frontiersin.org
The fragile X mental retardation protein (FMRP) is an RNA-binding protein that regulates
mRNA metabolism. FMRP has been largely studied in the brain, where the absence of this�…

Novel FMRP interaction networks linked to cellular stress

MS Taha, F Haghighi, A Stefanski…�- The FEBS�…, 2021 - Wiley Online Library
Silencing of the fragile X mental retardation 1 (FMR1) gene and consequently lack of
synthesis of FMR protein (FMRP) are associated with fragile X syndrome, which is one of the�…

Methylation regulates the intracellular protein-protein and protein-RNA interactions of FMRP

N Dolzhanskaya, G Merz, JM Aletta…�- Journal of cell�…, 2006 - journals.biologists.com
FMRP, the fragile X mental retardation protein, is an RNA-binding protein that interacts
with∼ 4% of fetal brain mRNA. We have recently shown that a methyltransferase (MT) co�…

A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies

Y Kang, Y Zhou, Y Li, Y Han, J Xu, W Niu, Z Li…�- Nature�…, 2021 - nature.com
Fragile X syndrome (FXS) is caused by the loss of fragile X mental retardation protein
(FMRP), an RNA-binding protein that can regulate the translation of specific mRNAs. In this�…

Regulatory discrimination of mRNAs by FMRP controls mouse adult neural stem cell differentiation

B Liu, Y Li, EE Stackpole, A Novak…�- Proceedings of the�…, 2018 - National Acad Sciences
Fragile X syndrome (FXS) is caused by the loss of fragile X mental retardation protein
(FMRP), an RNA binding protein whose deficiency impacts many brain functions, including�…

[HTML][HTML] Widespread alterations in translation elongation in the brain of juvenile Fmr1 knockout mice

SD Sharma, JB Metz, H Li, BD Hobson, N Hornstein…�- Cell reports, 2019 - cell.com
FMRP (fragile X mental retardation protein) is a polysome-associated RNA-binding protein
encoded by Fmr1 that is lost in fragile X syndrome. Increasing evidence suggests that FMRP�…