Literature DB >> 8341591

A novel Brn3-like POU transcription factor expressed in subsets of rat sensory and spinal cord neurons.

N N Ninkina1, G E Stevens, J N Wood, W D Richardson.   

Abstract

Brn3a and Brn3b are mammalian members of the POU class of transcription factors. They are closely related to each other and to Unc86, which determines the normal development of certain cells, including mechanoreceptive sensory neurons in Caenorhabditis elegans. We screened a rat dorsal root ganglion (DRG) cDNA library at moderate stringency with a Brn3a POU-domain probe and identified a novel transcript encoding a POU protein that we have named Brn3c. Brn3c closely resembles Brn3a and Brn3b in its POU-domain and thus helps define a family of Unc86-related mammalian POU factors. Both Brn3a and Brn3c are expressed only in the central and peripheral nervous systems. In the neonatal rat, northern blots revealed a 3.6 kb Brn3a transcript in DRG, spinal cord and hindbrain, and a 2.6 kb Brn3c transcript in DRG and spinal cord. In situ hybridization showed that most DRG neurons express Brn3a whereas only a small subset of neurons expresses Brn3c. In the spinal cord, Brn3a is expressed by many dorsal horn neurons. In contrast, Brn3c is expressed by a very small number of cells in laminae 4/5 of the dorsal horn. These data suggest that Brn3-related POU factors may be involved in the development or function of particular subclasses of sensory and spinal cord neurons.

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Year:  1993        PMID: 8341591      PMCID: PMC309752          DOI: 10.1093/nar/21.14.3175

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  20 in total

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Authors:  A Goldsborough; A Ashworth; K Willison
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2.  A general method for isolation of high molecular weight DNA from eukaryotes.

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3.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

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4.  The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products.

Authors:  W Herr; R A Sturm; R G Clerc; L M Corcoran; D Baltimore; P A Sharp; H A Ingraham; M G Rosenfeld; M Finney; G Ruvkun
Journal:  Genes Dev       Date:  1988-12       Impact factor: 11.361

5.  The C. elegans cell lineage and differentiation gene unc-86 encodes a protein with a homeodomain and extended similarity to transcription factors.

Authors:  M Finney; G Ruvkun; H R Horvitz
Journal:  Cell       Date:  1988-12-02       Impact factor: 41.582

6.  Quantitative analysis of in situ hybridization methods for the detection of actin gene expression.

Authors:  J B Lawrence; R H Singer
Journal:  Nucleic Acids Res       Date:  1985-03-11       Impact factor: 16.971

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8.  A family of octamer-specific proteins present during mouse embryogenesis: evidence for germline-specific expression of an Oct factor.

Authors:  H R Schöler; A K Hatzopoulos; R Balling; N Suzuki; P Gruss
Journal:  EMBO J       Date:  1989-09       Impact factor: 11.598

9.  PDGF A chain homodimers drive proliferation of bipotential (O-2A) glial progenitor cells in the developing rat optic nerve.

Authors:  N Pringle; E J Collarini; M J Mosley; C H Heldin; B Westermark; W D Richardson
Journal:  EMBO J       Date:  1989-04       Impact factor: 11.598

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Authors:  N P Pringle; W D Richardson
Journal:  Development       Date:  1993-02       Impact factor: 6.868

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  28 in total

1.  Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development.

Authors:  M Xiang; L Gan; D Li; Z Y Chen; L Zhou; B W O'Malley; W Klein; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

2.  Alternative splicing of the Brn-3a and Brn-3b transcription factor RNAs is regulated in neuronal cells.

Authors:  Y Z Liu; S J Dawson; D S Latchman
Journal:  J Mol Neurosci       Date:  1996       Impact factor: 3.444

3.  The N-terminal domain unique to the long form of the Brn-3a transcription factor is essential to protect neuronal cells from apoptosis and for the activation of Bbcl-2 gene expression.

Authors:  M D Smith; S J Dawson; L M Boxer; D S Latchman
Journal:  Nucleic Acids Res       Date:  1998-09-15       Impact factor: 16.971

4.  The ability of POU family transcription factors to activate or repress gene expression is dependent on the spacing and context of their specific response elements.

Authors:  S J Dawson; Y Z Liu; B Rodel; T Möröy; D S Latchman
Journal:  Biochem J       Date:  1996-03-01       Impact factor: 3.857

5.  The Brn-3a transcription factor induces neuronal process outgrowth and the coordinate expression of genes encoding synaptic proteins.

Authors:  M D Smith; S J Dawson; D S Latchman
Journal:  Mol Cell Biol       Date:  1997-01       Impact factor: 4.272

6.  Transcription Factor Brn-3b Overexpression Enhances Neurite Outgrowth in PC12 Cells Under Condition of Hypoxia.

Authors:  Nitasha R Phatak; Dorota L Stankowska; Raghu R Krishnamoorthy
Journal:  Cell Mol Neurobiol       Date:  2015-03-19       Impact factor: 5.046

7.  Expression of P450c17 in the human fetal nervous system.

Authors:  Marcus D Schonemann; Marcus O Muench; Meng Kian Tee; Walter L Miller; Synthia H Mellon
Journal:  Endocrinology       Date:  2012-03-20       Impact factor: 4.736

8.  Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling.

Authors:  M Xiang; L Gan; L Zhou; W H Klein; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

9.  Transcription factor interactions and chromatin modifications associated with p53-mediated, developmental repression of the alpha-fetoprotein gene.

Authors:  Thi T Nguyen; Kyucheol Cho; Sabrina A Stratton; Michelle Craig Barton
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10.  Mouse Brn-3 family of POU transcription factors: a new aminoterminal domain is crucial for the oncogenic activity of Brn-3a.

Authors:  T Theil; S McLean-Hunter; M Zörnig; T Möröy
Journal:  Nucleic Acids Res       Date:  1993-12-25       Impact factor: 16.971

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