A spontaneous mutation affects programmed cell death during development of the rat eye

Debasish Sinha, Stacey Hose, Cheng Zhang, Rachel Neal, Madhumita Ghosh, Terrence P. O'Brien, Olof Sundin, Morton F. Goldberg, W. Gerald Robison, Paul Russell, Woo Kuen Lo, J. Samuel Zigler

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

We have discovered a spontaneous mutation in the Sprague-Dawley rat with a novel eye phenotype that we have named Nuc1. The Nuc1 mutation behaves as a single semi-dominant locus with an intermediate phenotype in the heterozygotes. Heterozygotes exhibit nuclear cataracts. Homozygous Nuc1 rats are fully viable and have microphthalmia, retinal abnormalities and disruption of lens structure shortly before birth. The homozygous mutant shows no obvious pathology outside of the eye, indicating that the mutation is highly eye specific in its effects. An unusual feature of the mutation is that it prevents the normal programmed loss of nuclei from lens fiber cells, but does not affect the loss of other organelles. TUNEL, light, and electron microscopic studies show normal intact nuclei in lens fibers, in contrast to many other models with degenerate nuclei and unlike normal lenses where no such nuclei remain. The beaded filament protein, filensin, is down-regulated in fibers of Nuc1, while heat shock cognate 70 is up-regulated. Homozygous retinas are thicker than normal, and TUNEL labeling indicates roughly half the number of apoptotic cells compared to a wild-type retina. The transient layer of Chievitz persists in adult Nuc1 retina, indicative of delayed development. Hence, Nuc1 is a novel mutation that could be an eye-specific regulator of apoptosis.

Original languageEnglish (US)
Pages (from-to)323-335
Number of pages13
JournalExperimental Eye Research
Volume80
Issue number3
DOIs
StatePublished - Mar 2005
Externally publishedYes

Fingerprint

Cell Death
Lenses
Mutation
Retina
In Situ Nick-End Labeling
Heterozygote
Microphthalmos
Phenotype
Organelles
Cataract
Sprague Dawley Rats
Shock
Cell Count
Hot Temperature
Parturition
Electrons
Apoptosis
Pathology
Light
Proteins

Keywords

  • Abnormal development of retina
  • Apoptosis
  • Eye development
  • Lens denucleation

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems

Cite this

A spontaneous mutation affects programmed cell death during development of the rat eye. / Sinha, Debasish; Hose, Stacey; Zhang, Cheng; Neal, Rachel; Ghosh, Madhumita; O'Brien, Terrence P.; Sundin, Olof; Goldberg, Morton F.; Robison, W. Gerald; Russell, Paul; Lo, Woo Kuen; Zigler, J. Samuel.

In: Experimental Eye Research, Vol. 80, No. 3, 03.2005, p. 323-335.

Research output: Contribution to journalArticle

Sinha, D, Hose, S, Zhang, C, Neal, R, Ghosh, M, O'Brien, TP, Sundin, O, Goldberg, MF, Robison, WG, Russell, P, Lo, WK & Zigler, JS 2005, 'A spontaneous mutation affects programmed cell death during development of the rat eye', Experimental Eye Research, vol. 80, no. 3, pp. 323-335. https://doi.org/10.1016/j.exer.2004.09.014
Sinha, Debasish ; Hose, Stacey ; Zhang, Cheng ; Neal, Rachel ; Ghosh, Madhumita ; O'Brien, Terrence P. ; Sundin, Olof ; Goldberg, Morton F. ; Robison, W. Gerald ; Russell, Paul ; Lo, Woo Kuen ; Zigler, J. Samuel. / A spontaneous mutation affects programmed cell death during development of the rat eye. In: Experimental Eye Research. 2005 ; Vol. 80, No. 3. pp. 323-335.
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