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Gsh-1: a novel murine homeobox gene expressed in the central nervous system

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TLDR
The characterization of Gsh‐1, a novel murine homeobox gene, is reported, with a transcript of approximately 2 kb in size present at embryonic days 10.5 to E13.5 and the consensus DNA ninding site of the GSh‐1 homeoprotein is determined to be GCT/CA/CATTAG/A.
Abstract
We report the characterization of Gsh-1, a novel murine homeobox gene. Northern blot analysis revealed a transcript of approximately 2 kb in size present at embryonic days 10.5, 11.5, and 12.5 of development. The cDNA sequence encoded a proline rich motif, a polyalanine tract, and a homeodomain with strong homology to those encoded by the clustered Hox genes. The Gsh-1 expression pattern was determined for days E8.5 to E13.5 by whole mount and serial section in situ hybridizations. Gsh-1 transcription was restricted to the central nervous system. Expression is present in the neural tube and hindbrain as two continuous, bilaterally symmetrical stripes within neural epithelial tissue. In the mesencephalon, expression is seen as a band across the most anterior portion. There is also diencephalon expression in the anlagen of the thalamus and the hypothalamus as well as in the optic stalk, optic recess, and the ganglionic eminence. Moreover, through the use of fusion proteins containing the Gsh-1 homeodomain, we have determined the consensus DNA ninding site of the Gsh-1 homeoprotein to be GCT/CA/CATTAG/A. ©1995 Wiley-Liss, Inc.

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Gsh2 and Pax6 play complementary roles in dorsoventral patterning of the mammalian telencephalon

TL;DR: Evidence is presented that the progenitor and postmitotic cells flanking the pallial/subpallial boundary (PSB) in the embryonic mouse can be subdivided into multiple regions that express unique combinations of transcription factors.
Journal ArticleDOI

Genetic control of dorsal-ventral identity in the telencephalon: opposing roles for Pax6 and Gsh2.

TL;DR: Results demonstrate that Pax6 and Gsh2 govern cortical and striatal development by regulating genetically opposing programs that control the expression of each other as well as the regionally expressed developmental regulators Mash1, the neurogenins and Dlx genes in telencephalic progenitors.
Journal ArticleDOI

Multiple Dorsoventral Origins of Oligodendrocyte Generation in the Spinal Cord and Hindbrain

TL;DR: It is proposed that oligodendrocytes derive from several distinct positional origins and that the activation of Olig1/2 at different positions is controlled by distinct genetic programs.
Journal ArticleDOI

Ventral neural patterning by Nkx homeobox genes: Nkx6.1 controls somatic motor neuron and ventral interneuron fates

TL;DR: The patterns of neurogenesis in mice carrying a targeted mutation in Nkx6.1 show a dorsal-to-ventral switch in the identity of progenitors and in the fate of postmitotic neurons, demonstrating the essential functions of NkX6.
Journal ArticleDOI

Pax-6 functions in boundary formation and axon guidance in the embryonic mouse forebrain.

TL;DR: It is concluded that Pax-6 plays multiple roles in forebrain patterning, including boundary formation, regionally restricted patterns in the developing brain and eye, neuron specification and axon guidance.
References
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Journal ArticleDOI

Transgenic mice overexpressing the mouse homoeobox-containing gene Hox-1.4 exhibit abnormal gut development

TL;DR: A construct carrying the mouse Hox-1.4 gene was introduced into the germ line of mice to begin to identify the m-acting elements required for proper expression and to assess the consequences of increasing Hox -1.
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Position-dependent expression of two related homeobox genes in developing vertebrate limbs

TL;DR: Results reported here indicate that both genes are rapidly activated by a signal from the apical ectoderm, which strongly suggest that Hox-7.1 and H Cox-8.1 have fundamental roles in limb-pattern formation.
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Hox genes and regionalization of the nervous system.

TL;DR: The main purpose of this review is to explore the relationship of the Hox genes to regionaiization and segmental pattern formation in the eNS, with particular emphasis on the hindbrain.
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Expression of the murine Dlx-1 homeobox gene during facial, ocular and limb development

TL;DR: This gene harbors a homeodomain related to that found in the Drosophila distal-less (dll) gene that is transcribed in several structures containing cells of neural crest origin such as the facial mesenchyme and various elements of the peripheral nervous system.
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Homeotic transformations in the mouse induced by overexpression of a human Hox3.3 transgene.

TL;DR: A permanent transgenic mouse line was generated carrying 40 copies of the human Hox3.3 gene, which causes homeotic transformations of the skeleton, in particular the appearance of an extra pair of ribs in the lumbar region, transformation of the shape of posterior ribs into that of more anterior ones, and the joining of an additional Pair of ribs to the sternum.
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