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Dlx1/2 are Central and Essential Components in the Transcriptional Code for Generating Olfactory Bulb Interneurons.

Cerebral cortex (New York, N.Y. : 1991) (2019-02-24)
Teng Guo, Guoping Liu, Heng Du, Yan Wen, Song Wei, Zhenmeiyu Li, Guangxu Tao, Zicong Shang, Xiaolei Song, Zhuangzhi Zhang, Zhejun Xu, Yan You, Bin Chen, John L Rubenstein, Zhengang Yang
RÉSUMÉ

Generation of olfactory bulb (OB) interneurons requires neural stem/progenitor cell specification, proliferation, differentiation, and young interneuron migration and maturation. Here, we show that the homeobox transcription factors Dlx1/2 are central and essential components in the transcriptional code for generating OB interneurons. In Dlx1/2 constitutive null mutants, the differentiation of GSX2+ and ASCL1+ neural stem/progenitor cells in the dorsal lateral ganglionic eminence is blocked, resulting in a failure of OB interneuron generation. In Dlx1/2 conditional mutants (hGFAP-Cre; Dlx1/2F/- mice), GSX2+ and ASCL1+ neural stem/progenitor cells in the postnatal subventricular zone also fail to differentiate into OB interneurons. In contrast, overexpression of Dlx1&2 in embryonic mouse cortex led to ectopic production of OB-like interneurons that expressed Gad1, Sp8, Sp9, Arx, Pbx3, Etv1, Tshz1, and Prokr2. Pax6 mutants generate cortical ectopia with OB-like interneurons, but do not do so in compound Pax6; Dlx1/2 mutants. We propose that DLX1/2 promote OB interneuron development mainly through activating the expression of Sp8/9, which further promote Tshz1 and Prokr2 expression. Based on this study, in combination with earlier ones, we propose a transcriptional network for the process of OB interneuron development.

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Anticorps anti-Olig-2, Chemicon®, from rabbit
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Anticorps anti-Gsh2, serum, from rabbit
Sigma-Aldrich
Anti-EBF-1 Antibody, from rabbit, purified by affinity chromatography
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ANTI-GSX2 (C-TERM) antibody produced in rabbit, IgG fraction of antiserum, buffered aqueous solution