Divergent functions of the proneural genes Mash1 and Ngn2 in the specification of neuronal subtype identity

被引:291
作者
Parras, CM
Schuurmans, C
Scardigli, R
Kim, J
Anderson, DJ
Guillemot, F [1 ]
机构
[1] Univ Strasbourg 1, INSERM,CU Strasbourg, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[2] CALTECH, Howard Hughes Med Inst, Div Biol 216 76, Pasadena, CA 91125 USA
关键词
knock-in mutations; bHLH factors; CNS; PNS; neuronal specification;
D O I
10.1101/gad.940902
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The neural bHLH genes Mash1 and Ngn2 are expressed in complementary populations of neural progenitors in the central and peripheral nervous systems. Here, we have systematically compared the activities of the two genes during neural development by generating replacement mutations in mice in which the coding sequences of Mash1 and Ngn2 were swapped. Using this approach, we demonstrate that Mash1 has the capacity to respecify the identity of neuronal populations normally derived from Ngn2-expressing progenitors in the dorsal telencephalon and ventral spinal cord. In contrast, misexpression of Ngn2 in Mash1-expressing progenitors does not result in any overt change in neuronal phenotype. Taken together, these results demonstrate that Mash1 and Ngn2 have divergent functions in specification of neuronal subtype identity, with Mash1 having the characteristics of an instructive determinant whereas Ngn2 functions as a permissive factor that must act in combination with other factors to specify neuronal phenotypes. Moreover, the ectopic expression of Ngn2 can rescue the neurogenesis defects of Mash1 null mutants in the ventral telencephalon and sympathetic ganglia but not in the ventral spinal cord and the locus coeruleus, indicating that Mash1 contribution to the specification of neuronal fates varies greatly in different lineages, presumably depending on the presence of other determinants of neuronal identity.
引用
收藏
页码:324 / 338
页数:15
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