PFKM

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PFKM ou PFK-M (do inglês phosphofructokinase, muscle, músculo fosfofrutoquinase) é um gene humano.1

Mutações neste gene resultam em miopatia metabólica caracterizada por intolerância ao exercício e hemólise2 e deficiência na fosfofrutoquinase nos eritrócitos3 .

Referências[editar | editar código-fonte]

  1. PFKM phosphofructokinase, muscle ( Homo sapiens ) - www.ncbi.nlm.nih.gov (em inglês)
  2. Nina Raben, Jeffrey B. Sherman; Mutations in muscle phosphofructokinase gene; Human Mutation; Volume 6 Issue 1, Pages 1 - 6; Jun 2005 DOI 10.1002/humu.1380060102 - www3.interscience.wiley.com (em inglês)
  3. Kahn A, Etiemble J, Meienhofer MC, Bovin P.; Erythrocyte phosphofructokinase deficiency associated with an unstable variant of muscle phosphofructokinase.; Clin Chim Acta. 1975 Jun 20;61(3):415-9. - www.ncbi.nlm.nih.gov (em inglês)

Leitura de apoio[editar | editar código-fonte]

  • Raben N, Sherman JB. (1995). "Mutations in muscle phosphofructokinase gene.". Hum. Mutat. 6 (1): 1–6. DOI:10.1002/humu.1380060102. PMID 7550225.
  • Kahn A, Etiemble J, Meienhofer MC, Bovin P. (1975). "Erythrocyte phosphofructokinase deficiency associated with an unstable variant of muscle phosphofructokinase.". Clin. Chim. Acta 61 (3): 415–9. DOI:10.1016/0009-8981(75)90434-9. PMID 125160.
  • Zhao ZZ, Malencik DA, Anderson SR. (1991). "Protein-induced inactivation and phosphorylation of rabbit muscle phosphofructokinase.". Biochemistry 30 (8): 2204–16. DOI:10.1021/bi00222a026. PMID 1825608.
  • Yamasaki T, Nakajima H, Kono N, et al.. (1991). "Structure of the entire human muscle phosphofructokinase-encoding gene: a two-promoter system.". Gene 104 (2): 277–82. DOI:10.1016/0378-1119(91)90262-A. PMID 1833270.
  • Sharma PM, Reddy GR, Babior BM, McLachlan A. (1990). "Alternative splicing of the transcript encoding the human muscle isoenzyme of phosphofructokinase.". J. Biol. Chem. 265 (16): 9006–10. PMID 2140567.
  • Nakajima H, Kono N, Yamasaki T, et al.. (1990). "Genetic defect in muscle phosphofructokinase deficiency. Abnormal splicing of the muscle phosphofructokinase gene due to a point mutation at the 5'-splice site.". J. Biol. Chem. 265 (16): 9392–5. PMID 2140573.
  • Valdez BC, Chen Z, Sosa MG, et al.. (1989). "Human 6-phosphofructo-1-kinase gene has an additional intron upstream of start codon.". Gene 76 (1): 167–9. DOI:10.1016/0378-1119(89)90019-X. PMID 2526044.
  • Sharma PM, Reddy GR, Vora S, et al.. (1989). "Cloning and expression of a human muscle phosphofructokinase cDNA.". Gene 77 (1): 177–83. DOI:10.1016/0378-1119(89)90372-7. PMID 2526045.
  • Nakajima H, Noguchi T, Yamasaki T, et al.. (1987). "Cloning of human muscle phosphofructokinase cDNA.". FEBS Lett. 223 (1): 113–6. DOI:10.1016/0014-5793(87)80519-7. PMID 2822475.
  • Vora S, Seaman C, Durham S, Piomelli S. (1980). "Isozymes of human phosphofructokinase: identification and subunit structural characterization of a new system.". Proc. Natl. Acad. Sci. U.S.A. 77 (1): 62–6. DOI:10.1073/pnas.77.1.62. PMID 6444721.
  • Kahn A, Weil D, Cottreau D, Dreyfus JC. (1982). "Muscle phosphofructokinase deficiency in man: expression of the defect in blood cells and cultured fibroblasts.". Ann. Hum. Genet. 45 (Pt 1): 5–14. DOI:10.1111/j.1469-1809.1981.tb00300.x. PMID 6459054.
  • Vasconcelos O, Sivakumar K, Dalakas MC, et al.. (1995). "Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease.". Proc. Natl. Acad. Sci. U.S.A. 92 (22): 10322–6. DOI:10.1073/pnas.92.22.10322. PMID 7479776.
  • Tsujino S, Servidei S, Tonin P, et al.. (1994). "Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency.". Am. J. Hum. Genet. 54 (5): 812–9. PMID 7513946.
  • Raben N, Exelbert R, Spiegel R, et al.. (1995). "Functional expression of human mutant phosphofructokinase in yeast: genetic defects in French Canadian and Swiss patients with phosphofructokinase deficiency.". Am. J. Hum. Genet. 56 (1): 131–41. PMID 7825568.
  • Raben N, Sherman J, Miller F, et al.. (1993). "A 5' splice junction mutation leading to exon deletion in an Ashkenazic Jewish family with phosphofructokinase deficiency (Tarui disease).". J. Biol. Chem. 268 (7): 4963–7. PMID 8444874.
  • Howard TD, Akots G, Bowden DW. (1996). "Physical and genetic mapping of the muscle phosphofructokinase gene (PFKM): reassignment to human chromosome 12q.". Genomics 34 (1): 122–7. DOI:10.1006/geno.1996.0250. PMID 8661033.
  • Hamaguchi T, Nakajima H, Noguchi T, et al.. (1997). "Novel missense mutation (W686C) of the phosphofructokinase-M gene in a Japanese patient with a mild form of glycogenosis VII.". Hum. Mutat. 8 (3): 273–5. DOI:<273::AID-HUMU13>3.3.CO;2-4 10.1002/(SICI)1098-1004(1996)8:3<273::AID-HUMU13>3.3.CO;2-4. PMID 8889589.
  • Scherer PE, Lisanti MP. (1997). "Association of phosphofructokinase-M with caveolin-3 in differentiated skeletal myotubes. Dynamic regulation by extracellular glucose and intracellular metabolites.". J. Biol. Chem. 272 (33): 20698–705. DOI:10.1074/jbc.272.33.20698. PMID 9252390.
  • Ristow M, Vorgerd M, Möhlig M, et al.. (1998). "Deficiency of phosphofructo-1-kinase/muscle subtype in humans impairs insulin secretion and causes insulin resistance.". J. Clin. Invest. 100 (11): 2833–41. DOI:10.1172/JCI119831. PMID 9389749.
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