Literature DB >> 11001812

Neural and extraneural expression of the neuronal ceroid lipofuscinoses genes CLN1, CLN2, and CLN3: functional implications for CLN3.

S Chattopadhyay1, D A Pearce.   

Abstract

The neuronal ceroid lipofuscinoses (NCLs) are the most common neurodegenerative disorders of childhood. We have examined mRNA levels of the CLN1, CLN2, and CLN3 genes, which are associated with the infantile, late infantile, and juvenile forms of NCL in 64 different human tissues, and have grouped the results into gastrointestinal tract, central nervous system, glandular/secretory, muscle, and carcinoma tissue types. mRNA levels for CLN3 are highest in gastrointestinal tissue and are also high in glandular/secretory tissue, whereas mRNA levels for CLN1 and CLN2 do not appear to be preferentially elevated in any tissue type. The significance of extraneural expression of CLN3 is reviewed in the context of the function of the protein. Copyright 2000 Academic Press.

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Year:  2000        PMID: 11001812     DOI: 10.1006/mgme.2000.3056

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  9 in total

Review 1.  Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses.

Authors:  Sara E Mole; Ruth E Williams; Hans H Goebel
Journal:  Neurogenetics       Date:  2005-09-28       Impact factor: 2.660

2.  A novel deletion variant in CLN3 with highly variable expressivity is responsible for juvenile neuronal ceroid lipofuscinoses.

Authors:  Naser Gilani; Ehsan Razmara; Mehmet Ozaslan; Ihsan Kareem Abdulzahra; Saeid Arzhang; Ali Reza Tavasoli; Masoud Garshasbi
Journal:  Acta Neurol Belg       Date:  2021-03-30       Impact factor: 2.396

3.  Lysosomal degradation of cholecystokinin-(29-33)-amide in mouse brain is dependent on tripeptidyl peptidase-I: implications for the degradation and storage of peptides in classical late-infantile neuronal ceroid lipofuscinosis.

Authors:  Francesca Bernardini; Michael J Warburton
Journal:  Biochem J       Date:  2002-09-01       Impact factor: 3.857

4.  Altered glutamate receptor function in the cerebellum of the Ppt1-/- mouse, a murine model of infantile neuronal ceroid lipofuscinosis.

Authors:  Rozzy Finn; Attila D Kovács; David A Pearce
Journal:  J Neurosci Res       Date:  2011-10-04       Impact factor: 4.164

5.  Decreased sensitivity of palmitoyl protein thioesterase 1-deficient neurons to chemical anoxia.

Authors:  Meredith Meyer; Attila D Kovács; David A Pearce
Journal:  Metab Brain Dis       Date:  2016-10-08       Impact factor: 3.584

Review 6.  The neuronal ceroid lipofuscinoses: mutations in different proteins result in similar disease.

Authors:  Jill M Weimer; Elizabeth Kriscenski-Perry; Yasser Elshatory; David A Pearce
Journal:  Neuromolecular Med       Date:  2002       Impact factor: 4.103

Review 7.  Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses.

Authors:  Anil B Mukherjee; Abhilash P Appu; Tamal Sadhukhan; Sydney Casey; Avisek Mondal; Zhongjian Zhang; Maria B Bagh
Journal:  Mol Neurodegener       Date:  2019-01-16       Impact factor: 14.195

8.  Mice deficient in the lysosomal enzyme palmitoyl-protein thioesterase 1 (PPT1) display a complex retinal phenotype.

Authors:  Yevgeniya Atiskova; Susanne Bartsch; Tatyana Danyukova; Elke Becker; Christian Hagel; Stephan Storch; Udo Bartsch
Journal:  Sci Rep       Date:  2019-10-02       Impact factor: 4.379

Review 9.  The CLN3 gene and protein: What we know.

Authors:  Myriam Mirza; Anna Vainshtein; Alberto DiRonza; Uma Chandrachud; Luke J Haslett; Michela Palmieri; Stephan Storch; Janos Groh; Niv Dobzinski; Gennaro Napolitano; Carolin Schmidtke; Danielle M Kerkovich
Journal:  Mol Genet Genomic Med       Date:  2019-09-30       Impact factor: 2.183

  9 in total

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