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Ilf3 and NF90 associate with the axonal targeting element of Tau mRNA
被引:47
作者:
Larcher, JC
Gasmi, L
Viranaïcken, W
Eddé, B
Bernard, R
Ginzburg, I
Denoulet, P
机构:
[1] Univ Paris 06, Biochim Cellulaire Lab, CNRS, UMR 7098, F-75252 Paris 05, France
[2] CRBM, CNRS, UPR 1086, F-34293 Montpellier, France
[3] Univ Paris 06, CNRS, UMR 7101, F-75252 Paris 05, France
[4] Weizmann Inst Sci, Dept Neurobiol, IL-76100 Rehovot, Israel
关键词:
microtubule;
protein-RNA interactions;
Northwestern blotting;
mRNA trafficking;
2-D PAGE;
D O I:
10.1096/fj.04-1763fje
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In neurons, the selective translocation of Tau mRNA toward axons is due to the presence of a nucleotide sequence located in its 3' untranslated region and serving as axonal targeting element. Using this RNA sequence as a probe by a Northwestern approach, we have detected several proteins that interact with the targeting RNA element and could potentially be involved in Tau mRNA translocation, translation halting, and/or stabilization. Among them, two proteins were identified as the interleukin enhancer binding factor 3 (Ilf3) and NF90, two isoforms derived from a single gene product through alternative splicing. Each protein comprises two double-stranded RNA binding motifs that can interact with the predicted stem-loop secondary structure of the axonal targeting element. Specific antibodies raised against common or specific peptide sequences showed that both Ilf3 and NF90 are polymorphic proteins that are detected in neuronal nuclei and cell bodies, as well as in the proximal neuritic segments. This observation favors the idea that Ilf3 and NF90 are part of a protein complex that escorts Tau mRNA toward the axon.
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页码:1761 / +
页数:24
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