Novel RNA- and FMRP-binding protein TRF2-S regulates axonal mRNA transport and presynaptic plasticity

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作者
Peisu Zhang
Kotb Abdelmohsen
Yong Liu
Kumiko Tominaga-Yamanaka
Je-Hyun Yoon
Grammatikakis Ioannis
Jennifer L. Martindale
Yongqing Zhang
Kevin G. Becker
In Hong Yang
Myriam Gorospe
Mark P. Mattson
机构
[1] Laboratory of Neurosciences,Department of Biomedical Engineering
[2] National Institute on Aging Intramural Research Program,Department of Neuroscience
[3] National Institutes of Health,undefined
[4] 251 Bayview Boulevard,undefined
[5] Baltimore,undefined
[6] Maryland 21224,undefined
[7] USA,undefined
[8] Laboratory of Genetics,undefined
[9] National Institute on Aging Intramural Research Program,undefined
[10] National Institutes of Health,undefined
[11] 251 Bayview Boulevard,undefined
[12] Baltimore,undefined
[13] Maryland 21224,undefined
[14] USA,undefined
[15] National University of Singapore,undefined
[16] SINAPSE,undefined
[17] National University of Singapore,undefined
[18] Johns Hopkins University School of Medicine,undefined
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Despite considerable evidence that RNA-binding proteins (RBPs) regulate mRNA transport and local translation in dendrites, roles for axonal RBPs are poorly understood. Here we demonstrate that a non-telomeric isoform of telomere repeat-binding factor 2 (TRF2-S) is a novel RBP that regulates axonal plasticity. TRF2-S interacts directly with target mRNAs to facilitate their axonal delivery. The process is antagonized by fragile X mental retardation protein (FMRP). Distinct from the current RNA-binding model of FMRP, we show that FMRP occupies the GAR domain of TRF2-S protein to block the assembly of TRF2-S–mRNA complexes. Overexpressing TRF2-S and silencing FMRP promotes mRNA entry to axons and enhances axonal outgrowth and neurotransmitter release from presynaptic terminals. Our findings suggest a pivotal role for TRF2-S in an axonal mRNA localization pathway that enhances axon outgrowth and neurotransmitter release.
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