Literature DB >> 15629700

Morphogenetic and cellular movements that shape the mouse cerebellum; insights from genetic fate mapping.

Sema K Sgaier1, Sandrine Millet, Melissa P Villanueva, Frada Berenshteyn, Christian Song, Alexandra L Joyner.   

Abstract

We used the cerebellum as a model to study the morphogenetic and cellular processes underlying the formation of elaborate brain structures from a simple neural tube, using an inducible genetic fate mapping approach in mouse. We demonstrate how a 90 degrees rotation between embryonic days 9 and 12 converts the rostral-caudal axis of dorsal rhombomere 1 into the medial-lateral axis of the wing-like bilateral cerebellar primordium. With the appropriate use of promoters, we marked specific medial-lateral domains of the cerebellar primordium and derived a positional fate map of the murine cerebellum. We show that the adult medial cerebellum is produced by expansion, rather than fusion, of the thin medial primordium. Furthermore, ventricular-derived cells maintain their original medial-lateral coordinates into the adult, whereas rhombic lip-derived granule cells undergo lateral to medial posterior transverse migrations during foliation. Thus, we show that progressive changes in the axes of the cerebellum underlie its genesis.

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Year:  2005        PMID: 15629700     DOI: 10.1016/j.neuron.2004.12.021

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  85 in total

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Journal:  Development       Date:  2007-06       Impact factor: 6.868

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6.  The Engrailed homeobox genes determine the different foliation patterns in the vermis and hemispheres of the mammalian cerebellum.

Authors:  Yulan Cheng; Anamaria Sudarov; Kamila U Szulc; Sema K Sgaier; Daniel Stephen; Daniel H Turnbull; Alexandra L Joyner
Journal:  Development       Date:  2010-02       Impact factor: 6.868

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9.  Common partner Smad-independent canonical bone morphogenetic protein signaling in the specification process of the anterior rhombic lip during cerebellum development.

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10.  Defects in the cerebella of conditional Neurod1 null mice correlate with effective Tg(Atoh1-cre) recombination and granule cell requirements for Neurod1 for differentiation.

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