The neuronal ceroid lipofuscinoses, collectively referred to as Batten disease, make up a group of inherited childhood disorders that result in blindness, motor and cognitive regression, brain atrophy, and seizures, ultimately leading to premature death. So far more than 10 genes have been implicated in different forms of the neuronal ceroid lipofuscinoses. Most related research has involved mouse models, but several naturally occurring large animal models have recently been discovered. In this review, we discuss the different large animal models and their significance in Batten disease research.
WilliamsREMoleSE. New nomenclature and classification scheme for the neuronal ceroid lipofuscinoses. Neurology. 2012;79:183–191.
3.
FrugierTMitchellNLTammenI. A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3. Neurobiol Dis. 2008;29:306–315.
4.
JollyRDMartinusRDPalmerDN. Sheep and other animals with ceroid-lipofuscinoses: their relevance to Batten disease. Am J Med Genet. 1992;42:609–614.
5.
GettyALPearceDA. Interactions of the proteins of neuronal ceroid lipofuscinosis: clues to function. Cell Mol Life Sci. 2011;68:453–474.
6.
WeimerJMCusterAWBenedictJW. Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons. Neurobiol Dis. 2006;22:284–293.
7.
KatzMLKhanSAwanoT. A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis. Biochem Biophys Res Commun. 2005;327:541–547.
8.
LingaasFAarskaugTSlettenM. Genetic markers linked to neuronal ceroid lipofuscinosis in English setter dogs. Anim Genet. 1998;29:371–376.
9.
ShibuyaHLiuPCKatzML. Coding sequence and exon/intron organization of the canine CLN3 (Batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs. J Neurosci Res. 1998;52:268–275.
10.
MelvilleSAWilsonCLChiangCS. A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs. Genomics. 2008;86:287–294.
11.
EvansJKatzMLLevesqueD. A variant form of neuronal ceroid lipofuscinosis in American bulldogs. J Vet Intern Med. 2005;19:44–51.
12.
AwanoTKatzMLO'BrienDP. A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis. Mol Genet Metab. 2006;87:341–348.
13.
AbitbolMThibaudJLOlbyNJ. A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis. Proc Natl Acad Sci U S A. 2010;107:14775–14780.
14.
OlbyNBlotSThibaudJL. Cerebellar cortical degeneration in adult American Staffordshire Terriers. J Vet Intern Med. 2004;18:201–208.
15.
FariasFHZengRJohnsonGS. A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. Neurobiol Disord. 2011;42:468–474.
16.
WöhlkeAPhillipUBockP. A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. PLoS Genet. 2011;7:e1002304.
17.
CummingsJFde LahuntaA. An adult case of canine neuronal ceroid-lipofuscinosis. Acta Neuropathol. 1977;39:43–51.
18.
VandeveldeMFatzerR. Neuronal ceroid-lipofuscinosis in older dachshunds. Vet Pathol. 1980;17:686–692.
19.
AwanoTKatzMLO’BrienDP. A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis. Mol Genet Metab. 2006;89:254–260.
20.
SandersDNFariasFHJohnsonGS. A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund. Mol Genet Metab. 2010:100:349–356.
21.
VuillemenotBRKatzMLCoatesJR. Intrathecal tripeptidyl-peptidase 1 reduces lysosomal storage in a canine model of late infantile neuronal ceroid lipofuscinosis. Mol Genet Metab. 2011;104:325–337.
22.
O’BrienDPKatzML. Neuronal ceroid lipofuscinosis in 3 Australian shepherd littermates. J Vet Intern Med. 2008;22:572–475.
23.
KatzMLFariasFHSandersDN. A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis. J Biomed Biotech. 2011;2011:198042.
24.
JollyRDWestDM. Blindness in South Hampshire sheep: a neuronal ceroid lipofuscinosis. N Z Vet J. 1976;24:123.
25.
BroomMFZhouCBroomJE. Ovine neuronal ceroid lipofuscinosis: a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6. J Med Genet. 1998;35:717–721.
26.
TammenIHouwelingPJFrugierT. A missense mutation (c.184C>T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA. Biochim Biophys Acta. 2006;1762:898–905.
27.
CookRWJollyRDPalmerDN. Neuronal ceroid lipofuscinosis in Merino sheep. Aust Vet J. 2002;80:292–297.
28.
JollyRDArthurDGKayGWPalmerDN. Neuronal ceroid-lipofuscinosis in Borderdale sheep. N Z Vet J. 2002;50:199–202.
29.
FrugierTMitchellNLTammenI. A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3. Neurobiol Dis. 2008;29:306–315.
30.
TyyneläJSoharISleatDE. Congenital ovine neuronal ceroid lipofuscinosis—a cathepsin D deficiency with increased levels of the inactive enzyme. Eur J Paediatr Neurol. 2001;5(suppl A):43–45.
31.
TyyneläJSoharISleatDE. A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration. EMBO J. 2000;19:2786–2792.
32.
HarperPAWalkerKHHealyPJ. Neurovisceral ceroid-lipofuscinosis in blind Devon cattle. Acta Neuropathol. 1988;75:632–636.
33.
HouwelingPJCavanaghJAPalmerDN. Neuronal ceroid lipofuscinosis in Devon cattle is caused by a single base duplication (c.662dupG) in the bovine CLN5 gene. Biochim Biophys Acta. 2006;1762:890–897.