Regulation of MuSK Expression by a Novel Signaling Pathway.

Saved in:
Bibliographic Details
Title: Regulation of MuSK Expression by a Novel Signaling Pathway.
Authors: Chang-Hoon Kim1, Xiong, Wen C.2 wxiong@path.uab.edu, Lin Me, Wen C.1 lmei@nrc.uab.edu
Source: Journal of Biological Chemistry. 10/3/2003, Vol. 278 Issue 40, p38522-38527. 6p. 5 Diagrams, 8 Graphs.
Subjects: Protein-tyrosine kinases, Gene expression, Genetic transcription, Laboratory mice
Abstract: MuSK is a receptor tyrosine kinase essential for neuromuscular junction formation. Expression of the MuSK gene is tightly regulated during development and at the neuromuscular junction. However, little is known about molecular mechanisms regulating its gene expression. Here we report a characterization of the promoter of the mouse MuSK gene. The transcription of MuSK starts at multiple sites with a major site 51 nt upstream of the translation start site. We have identified an E-box-like cis-element that is both required and sufficient for differentiation-dependent transcription. Interestingly, the promoter activity of the MuSK gene did not respond to neuregulin, a factor believed to mediate the synapse-specific transcription of acetylcholine receptor subunit genes. Rather, MuSK expression is increased in muscle cells stimulated with Wnt or at conditions when the Wnt signaling was activated. These results suggest a novel mechanism for the MuSK synapse-specific expression. [ABSTRACT FROM AUTHOR]
Copyright of Journal of Biological Chemistry is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Engineering Source
FullText Text:
  Availability: 0
Header DbId: egs
DbLabel: Engineering Source
An: 11217511
AccessLevel: 6
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Regulation of MuSK Expression by a Novel Signaling Pathway.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Chang-Hoon+Kim%22">Chang-Hoon Kim</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Xiong%2C+Wen+C%2E%22">Xiong, Wen C.</searchLink><relatesTo>2</relatesTo><i> wxiong@path.uab.edu</i><br /><searchLink fieldCode="AR" term="%22Lin+Me%2C+Wen+C%2E%22">Lin Me, Wen C.</searchLink><relatesTo>1</relatesTo><i> lmei@nrc.uab.edu</i>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Journal+of+Biological+Chemistry%22">Journal of Biological Chemistry</searchLink>. 10/3/2003, Vol. 278 Issue 40, p38522-38527. 6p. 5 Diagrams, 8 Graphs.
– Name: Subject
  Label: Subjects
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Protein-tyrosine+kinases%22">Protein-tyrosine kinases</searchLink><br /><searchLink fieldCode="DE" term="%22Gene+expression%22">Gene expression</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+transcription%22">Genetic transcription</searchLink><br /><searchLink fieldCode="DE" term="%22Laboratory+mice%22">Laboratory mice</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: MuSK is a receptor tyrosine kinase essential for neuromuscular junction formation. Expression of the MuSK gene is tightly regulated during development and at the neuromuscular junction. However, little is known about molecular mechanisms regulating its gene expression. Here we report a characterization of the promoter of the mouse MuSK gene. The transcription of MuSK starts at multiple sites with a major site 51 nt upstream of the translation start site. We have identified an E-box-like cis-element that is both required and sufficient for differentiation-dependent transcription. Interestingly, the promoter activity of the MuSK gene did not respond to neuregulin, a factor believed to mediate the synapse-specific transcription of acetylcholine receptor subunit genes. Rather, MuSK expression is increased in muscle cells stimulated with Wnt or at conditions when the Wnt signaling was activated. These results suggest a novel mechanism for the MuSK synapse-specific expression. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Journal of Biological Chemistry is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=11217511
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1074/jbc.M305058200
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 6
        StartPage: 38522
    Subjects:
      – SubjectFull: Protein-tyrosine kinases
        Type: general
      – SubjectFull: Gene expression
        Type: general
      – SubjectFull: Genetic transcription
        Type: general
      – SubjectFull: Laboratory mice
        Type: general
    Titles:
      – TitleFull: Regulation of MuSK Expression by a Novel Signaling Pathway.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Chang-Hoon Kim
      – PersonEntity:
          Name:
            NameFull: Xiong, Wen C.
      – PersonEntity:
          Name:
            NameFull: Lin Me, Wen C.
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 03
              M: 10
              Text: 10/3/2003
              Type: published
              Y: 2003
          Identifiers:
            – Type: issn-print
              Value: 00219258
          Numbering:
            – Type: volume
              Value: 278
            – Type: issue
              Value: 40
          Titles:
            – TitleFull: Journal of Biological Chemistry
              Type: main
ResultId 1