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A Role for bHLH Transcription Factors in Retinal Degeneration and Dysfunction

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Retinal Degenerative Diseases

Part of the book series: Advances in Experimental Medicine and Biology ((volume 572))

Abstract

The basic helix loop helix (bHLH) transcription factors collectively mediate cellular differentiation in almost every type of tissue including the retina (Murre et al. 1989; Jan and Jan 1993; Cepko 1999). Class A factors are ubiquitously expressed throughout mammalian tissue, while the expression of class B factors are cell type specific. These factors have both a DNA binding domain and helix loop helix domain (HLH) protein dimerization domain. Class B factors usually heterodimerize with the ubiquitously expressed, bHLH factors, such as E12/E47. Because of their importance during photoreceptor development, bHLH factors are candidate genes for photoreceptor degeneration. We have examined the roles of two bHLH factors, both which are expressed during retinal development, but also share the property of continued expression in the adult retina.

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© 2006 Springer Science+Business Media, Inc.

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Pennesi, M.E., Bramblett, D.E., Cho, JH., Tsai, MJ., Wu, S.M. (2006). A Role for bHLH Transcription Factors in Retinal Degeneration and Dysfunction. In: Hollyfield, J.G., Anderson, R.E., LaVail, M.M. (eds) Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology, vol 572. Springer, Boston, MA. https://doi.org/10.1007/0-387-32442-9_23

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  • DOI: https://doi.org/10.1007/0-387-32442-9_23

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-387-28464-4

  • Online ISBN: 978-0-387-32442-5

  • eBook Packages: MedicineMedicine (R0)

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