Dendritic trafficking of BDNF mRNA is mediated by translin and blocked by the G196A (Val66Met) mutation

被引:173
作者
Chiaruttini, C. [1 ]
Vicario, A. [1 ]
Li, Z. [3 ]
Baj, G. [1 ]
Braiuca, P. [2 ]
Wu, Y. [3 ]
Lee, F. S. [4 ]
Gardossi, L. [2 ]
Baraban, J. M. [3 ]
Tongiorgi, E. [1 ]
机构
[1] Univ Trieste, Dept Life Sci, BRAIN Ctr Neurosci, I-34127 Trieste, Italy
[2] Univ Trieste, Dipartimento Sci Farmaceut, I-34127 Trieste, Italy
[3] Johns Hopkins Univ, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
[4] Cornell Weill Sch Med, Dept Psychiat, New York, NY 10065 USA
关键词
neuropsychiatric disorders; neurotrophins; NEUROTROPHIC FACTOR; HIPPOCAMPAL-NEURONS; BINDING COMPLEX; BRAIN; POLYMORPHISM; PROTEIN; LOCALIZATION; EXPRESSION; MORPHOLOGY; PATHWAY;
D O I
10.1073/pnas.0902833106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alternatively spliced brain-derived neurotrophic factor (BDNF) transcripts are targeted to distinct cellular compartments in neurons but the mechanisms underlying this sorting are unknown. Although only some BDNF isoforms are targeted to dendrites, we have found that the coding region common to all BDNF transcripts contains a constitutively active dendritic targeting signal and that this signal is suppressed in transcripts containing exons 1 or 4, which are restricted to the cell soma and proximal dendrites. This dendritic targeting signal is mediated by translin, an RNA-binding protein implicated in RNA trafficking, and is disrupted by the G196A mutation associated with memory deficits and psychiatric disorders. Molecular modeling and mutational studies indicate that the G196A mutation blocks dendritic targeting of BDNF mRNA by disrupting its interaction with translin. These findings implicate abnormal dendritic trafficking of BDNF mRNA in the pathophysiology of neuropsychiatric disorders linked to the G196A mutation.
引用
收藏
页码:16481 / 16486
页数:6
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