Splicing variants in sheep CLN3, the gene underlying juvenile neuronal ceroid lipofuscinosis

Mol Genet Metab. 1999 Jun;67(2):169-75. doi: 10.1006/mgme.1999.2848.

Abstract

Mutations in different genes underlie different forms of the neuronal ceroid lipofuscinoses (NCLs, Batten disease). Subunit c of mitochondrial ATP synthase specifically accumulates in most of them, including the juvenile CLN3 form and a sheep form orthologous to CLN6. Products of these genes are likely to be components of a complex or pathway for subunit c turnover, and their expression may be cross-regulated. Different bands, some with different subcellular distributions, were detected by antisera against different regions of CLN3 on Western blots of sheep tissues. Affected liver blots were the same as controls but a specific 50-kDa band was at higher concentration in affected brain homogenates than in controls. Others have also reported bands reacting differently to different CLN3 antibodies. When the 3' end of sheep CLN3 cDNA was amplified by RT-PCR, four mRNA splicing variants were found. Different CLN3 splicing variants at the 5' end of the human cDNA have been reported. These mRNA splicing variants may account the variation of epitope distribution and the different subcellular locations of the CLN3 gene product(s). The predicted size of the unmodified CLN3 protein is 48 kDa. Significantly higher molecular weight bands may correspond to oligomers of a CLN3 isoform or to a CLN3 isoform tightly bound to another protein.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Blotting, Western / veterinary
  • Genetic Variation
  • Humans
  • Liver / chemistry
  • Membrane Glycoproteins*
  • Molecular Chaperones*
  • Molecular Sequence Data
  • Molecular Weight
  • Neuronal Ceroid-Lipofuscinoses / genetics*
  • Peptides / chemical synthesis
  • Peptides / immunology
  • Protein Binding
  • Proteins / chemistry
  • Proteins / genetics*
  • Proteins / immunology
  • RNA Splicing / genetics*
  • RNA, Messenger / biosynthesis
  • Sequence Homology, Amino Acid
  • Sequence Homology, Nucleic Acid
  • Sheep / genetics*

Substances

  • CLN3 protein, human
  • Membrane Glycoproteins
  • Molecular Chaperones
  • Peptides
  • Proteins
  • RNA, Messenger