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PCM1

Introduction

Pericentriolar material 1, also known as PCM1, is a human gene.[1]

References

References

  1. ↑ “Entrez Gene: PCM1 pericentriolar material 1”.
Further reading

Further reading

  • Ohata H, Fujiwara Y, Koyama K, Nakamura Y (1995). “Mapping of the human autoantigen pericentriolar material 1 (PCM1) gene to chromosome 8p21.3-p22”. Genomics. 24 (2): 404–6. doi:10.1006/geno.1994.1640. PMID 7698772.
  • Balczon R, Bao L, Zimmer WE (1994). “PCM-1, A 228-kD centrosome autoantigen with a distinct cell cycle distribution”. J. Cell Biol. 124 (5): 783–93. PMID 8120099.
  • Engelender S, Sharp AH, Colomer V; et al. (1998). “Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin”. Hum. Mol. Genet. 6 (13): 2205–12. PMID 9361024.
  • Dias Neto E, Correa RG, Verjovski-Almeida S; et al. (2000). “Shotgun sequencing of the human transcriptome with ORF expressed sequence tags”. Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3491–6. PMID 10737800.
  • Corvi R, Berger N, Balczon R, Romeo G (2000). “RET/PCM-1: a novel fusion gene in papillary thyroid carcinoma”. Oncogene. 19 (37): 4236–42. doi:10.1038/sj.onc.1203772. PMID 10980597.
  • Li Q, Hansen D, Killilea A; et al. (2001). “Kendrin/pericentrin-B, a centrosome protein with homology to pericentrin that complexes with PCM-1”. J. Cell. Sci. 114 (Pt 4): 797–809. PMID 11171385.
  • Kumar S, Connor JR, Dodds RA; et al. (2001). “Identification and initial characterization of 5000 expressed sequenced tags (ESTs) each from adult human normal and osteoarthritic cartilage cDNA libraries”. Osteoarthr. Cartil. 9 (7): 641–53. doi:10.1053/joca.2001.0421. PMID 11597177.
  • Dammermann A, Merdes A (2002). “Assembly of centrosomal proteins and microtubule organization depends on PCM-1”. J. Cell Biol. 159 (2): 255–66. doi:10.1083/jcb.200204023. PMID 12403812.
  • Strausberg RL, Feingold EA, Grouse LH; et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.
  • Ansley SJ, Badano JL, Blacque OE; et al. (2003). “Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome”. Nature. 425 (6958): 628–33. doi:10.1038/nature02030. PMID 14520415.
  • Ota T, Suzuki Y, Nishikawa T; et al. (2004). “Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Kim JC, Badano JL, Sibold S; et al. (2004). “The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression”. Nat. Genet. 36 (5): 462–70. doi:10.1038/ng1352. PMID 15107855.
  • Brill LM, Salomon AR, Ficarro SB; et al. (2004). “Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry”. Anal. Chem. 76 (10): 2763–72. doi:10.1021/ac035352d. PMID 15144186.
  • Armes JE, Hammet F, de Silva M; et al. (2004). “Candidate tumor-suppressor genes on chromosome arm 8p in early-onset and high-grade breast cancers”. Oncogene. 23 (33): 5697–702. doi:10.1038/sj.onc.1207740. PMID 15184884.
  • Beausoleil SA, Jedrychowski M, Schwartz D; et al. (2004). “Large-scale characterization of HeLa cell nuclear phosphoproteins”. Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMID 15302935.
  • Ballif BA, Villén J, Beausoleil SA; et al. (2005). “Phosphoproteomic analysis of the developing mouse brain”. Mol. Cell Proteomics. 3 (11): 1093–101. doi:10.1074/mcp.M400085-MCP200. PMID 15345747.
  • Gerhard DS, Wagner L, Feingold EA; et al. (2004). “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.
  • Hames RS, Crookes RE, Straatman KR; et al. (2005). “Dynamic recruitment of Nek2 kinase to the centrosome involves microtubules, PCM-1, and localized proteasomal degradation”. Mol. Biol. Cell. 16 (4): 1711–24. doi:10.1091/mbc.E04-08-0688. PMID 15659651.
  • Reiter A, Walz C, Watmore A; et al. (2005). “The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2”. Cancer Res. 65 (7): 2662–7. doi:10.1158/0008-5472.CAN-04-4263. PMID 15805263.
  • Murati A, Gelsi-Boyer V, Adélaïde J; et al. (2005). “PCM1-JAK2 fusion in myeloproliferative disorders and acute erythroid leukemia with t(8;9) translocation”. Leukemia. 19 (9): 1692–6. doi:10.1038/sj.leu.2403879. PMID 16034466.

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