Cloning and characterization of the multiple murine homologues of NAIP (neuronal apoptosis inhibitory protein)

Genomics

Volumn 51, Issue 1, 1998, Pages 107-113

  Yaraghi, Zahra ^a,b   Korneluk, Robert G ^a,b   MacKenzie, Alex ^a,b  

^a CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^b UNIVERSITY OF OTTAWA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; GENE LOCUS; GENE SEQUENCE; GENE STRUCTURE; GENOME; HEREDITARY SPINAL MUSCULAR ATROPHY; MOLECULAR CLONING; MOUSE; NONHUMAN; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SOUTHERN BLOTTING;

EID: 0032127922     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5378     Document Type: Article

References (28)

1. Altschul S. F., Warren G., Miller W., Meyers E. W., Lipman D. J. Basic alignment search tool. J. Mol. Biol. 215:1990;403-410.
2. Barnes, D. G. Besner-Johnston, A. Gendron, N. Chen, Q. MacKenzie, A. 1998, A refined genomic map of the spinal muscular atrophy critical region.
3. Burghes A. H. M., Ingraham S. E., McLean M. D., Thompson T. G., McPherson J. D., Kote-Jarai Z., Carpten J. D., DiDonato C. J., Ikeda J.-E., Surh L., Wirth B., Sargent C. A., Ferguson-Smith M. A., Fuerst P., Moysis R. K., Grady D. L., Zerres K., Korneluk R. G., MacKenzie A. E., Wasmuth J. J. A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene. Genomics. 21:1994;394-402.
4. Burlet Ph., Buerglen L., Clermont O., Lefebvre S., Viollet L., Munnich A., Melki J. Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease. J. Med. Genet. 33:1996;281-283.
5. Chen Q., Baird S. D., Mahadevan M., Besner-Johnston A., Farahani R., Xuan J. Y., Kang X., Lefebvre C., Ikeda J.-E., Korneluk R. G., MacKenzie A. Sequence of a 131 kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP. Genomics. 48:1998;121-127.
6. Clem R. J., Miller L. K. Control of programmed cell death by the baculovirus genes p35 and iap. Mol. Cell. Biol. 14:1994;5212-5222.
7. Cobben J. M., van der Steege G., Grootscholten P., de Visser M., Scheffer H., Buys C. H. Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. Am. J. Hum. Genet. 57:1995;805-808.
8. Crook N. E., Clem R. J., Miller L. K. An apoptosis-inhibiting baculovirus gene with a zinc finger-like motif. J. Virol. 67:1993;2168-2174.
9. Dubowitz V. Muscle Disorders in Childhood. 1978;Saunders, East Sussex. p. 146-190.
10. Dubowitz V. Chaos in classification of the spinal muscular atrophies of childhood. Neuromusc. Disord. 1:1991;47-53.
11. Hahnen E., Forkert R., Marke C., Rudnik-Schoneborn S., Schonling J., Zerres K., Wirth B. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: Evidence of homozygous deletions of the SMN gene in unaffected individuals. Hum. Mol. Genet. 4:1995;1927-1933.
12. Lefebvre S., Buerglen L., Reboullet S., Clermont O., Burlet P., Viollet L., Benichou B., Cruad C., Millasseau P., Zeviani M., Le Paslier D., Frezal J., Cohen D., Weissenbach J., Munnich A., Melki J. Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 80:1995;155-165.
13. Lefebvre S., Burlet P., Liu Q., Bertrandy S., Clermont O., Munnich A., Dreyfuss G., Melki J. Correlation between severity and SMN protein level in spinal muscular atrophy. Nat. Genet. 16:1997;265-269.
14. Liston P., Roy N., Tamai K., Lefebvre C., Baird S., Cherton-Horvat G., Farahani R., McLean M. D., Ikeda J.-E., MacKenzie A. E., Korneluk R. G. Suppression of apoptosis in mammalian cells by NAIP and a related family of IAP genes. Nature. 379:1996;349-353.
15. McLean M. D., Roy N., MacKenzie A. E., Salih M., Burghes A., Simard L., Korneluk R. G., Ikeda J.-E., Surh L. Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type I spinal muscular atrophy. Hum. Mol. Genet. 3:1994;1951-1956.
16. Oppenheim R. W. Cell death during development of the nervous system. Annu. Rev. Neurosci. 14:1991;453-501.
17. Pearn J. H. Classification of spinal muscular atrophies. Lancet. i:1980;919-922.
18. Rajcan-Separovic E., Mahadevan M. S., Lefebvre C., Besner-Johnston A., Ikeda J.-E., Korneluk R. G., MacKenzie A. FISH detection of chromosomal polymorphisms and deletions in the spinal muscular atrophy (SMA) region of 5q13. Cytogenet. Cell Genet. 75:1996;243-247.
19. Rodrigues N. R., Owen N., Talbot K., Patel S., Muntoni F., Ignatius J., Dubowitz V., Davies K. E. Gene deletions in spinal muscular atrophy. J. Med. Genet. 33:1996;93-96.
20. Roy N., McLean M. D., Besner-Johnston A., Lefebvre C., Salih M., Carpenten J. D., Burghes A. H. M., Yaraghi Z., Ikeda J.-E., Korneluk R. G., MacKenzie A. E. Refined physical map of the spinal muscular atrophy gene (SMA) region at 5q13 based on YAC and cosmid contiguous arrays. Genomics. 26:1995a;451-460.
21. Roy N., Mahadevan M. S., McLean M. D., Shutler G., Yaraghi Z., Farahani R., Baird S., Besner-Johnston A., Lefebvre C., Kang X., Salih M., Tamai K., Guan X., Ioannou P., Crawford T., de Jong P. J., Surh L., Ikeda J.-E., Korneluk R. G., MacKenzie A. The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy. Cell. 80:1995b;167-178.
22. Sambrook J., Fritsch E. F., Maniatis T. Molecular Cloning: A Laboratory Manual. 1989;Cold Spring Harbor Laboratory Press, New York.
23. Scharf J. M., Damron D., Frisella A., Bruno S., Beggs A. H., Kunkel L. M., Dietrich W. F. The mouse region syntenic for human spinal muscular atrophy lies within theLgn1Naip. Genomics. 38:1996;405-417.
24. Shipley J. M., Klinkenberg M., Wu B. M., Bachinsky D. R., Grubb J. H., Sly W. S. Mutational analysis of patients with mucopolysaccharidosis type VII, and identification of pseudogenes. Am. J. Hum. Genet. 52:1993;517-526.
25. Theodosiou A. M., Morrison K. E., Nesbit A. M., Daniels R. J., Campbell L., Francis M. J., Christodoulou Z., Davies K. E. Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13. Am. J. Hum. Genet. 55:1994;1209-1217.
26. Thompson T. G., DiDonato C. J., Simard L. R., Ingraham S. E., Burghes A. H. M., Crawford T. O., Rochette C., Mendell J. R., Wasmuth J. J. A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients. Nat. Genet. 9:1995;56-62.
27. Xu D. G., Korneluk R. G., Tamai K., Wigle N., Hakim A., MacKenzie A., Robertson G. S. Distributionof neuronal apoptosis inhibitory protein-like immunoreactivity in the rat central nervous system. J. Comp. Neurol. 381:1997a;1-13.
28. Xu D. G., Crocker S. J., Doucet J.-P., St-Jean M., Tamai K., Hakim A., Ikeda J.-E., Liston P., Thompson C. S., Korneluk R. G., MacKenzie A., Robertson G. S. Elevation of neuronal expression of NAIP reduces ischemic damage in the hippocampus. Nat. Med. 3:1997b;997-1004.