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The Runx3 transcription factor regulates development and survival of TrkC dorsal root ganglia neurons
被引:373
作者:
Levanon, D
Bettoun, D
Harris-Cerruti, C
Woolf, E
Negreanu, V
Eilam, R
Bernstein, Y
Goldenberg, D
Xiao, CY
Fliegauf, M
Kremer, E
Otto, F
Brenner, O
Lev-Tov, A
Groner, Y
[1
]
机构:
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Vet Resources, IL-76100 Rehovot, Israel
[3] Hebrew Univ Jerusalem, Sch Med, Dept Anat & Cell Biol, IL-91120 Jerusalem, Israel
[4] Univ Freiburg, Med Ctr, Dept Hematol Oncol, D-79106 Freiburg, Germany
关键词:
knockout mice;
Runx1-TrkA;
sensory ataxia;
stretch reflex arc;
trigeminal ganglia;
D O I:
10.1093/emboj/cdf370
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:
The RUNX transcription factors are important regulators of linage-specific gene expression in major developmental pathways. Recently, we demonstrated that Runx3 is highly expressed in developing cranial and dorsal root ganglia (DRGs). Here we report that within the DRGs, Runx3 is specifically expressed in a subset of neurons, the tyrosine kinase receptor C (TrkC) proprioceptive neurons. We show that Runx3-deficient mice develop severe limb ataxia due to disruption of monosynaptic connectivity between intra spinal afferents and motoneurons. We demonstrate that the underlying cause of the defect is a loss of DRG proprioceptive neurons, reflected by a decreased number of TrkC-, parvalbumin- and beta-galactosidase-positive cells. Thus, Runx3 is a neurogenic TrkC neuron-specific transcription factor. In its absence, TrkC neurons in the DRG do not survive long enough to extend their axons toward target cells, resulting in lack of connectivity and ataxia. The data provide new genetic insights into the neurogenesis of DRGs and may help elucidate the molecular mechanisms underlying somatosensory-related ataxia in humans.
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页码:3454 / 3463
页数:10
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