CENPF

An Error has occured retrieving Wikidata item for infobox CENPF‏ (Centromere protein F) هوَ بروتين يُشَفر بواسطة جين CENPF في الإنسان.^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

^ Testa JR، Zhou JY، Bell DW، Yen TJ (مارس 1995). "Chromosomal localization of the genes encoding the kinetochore proteins CENPE and CENPF to human chromosomes 4q24→q25 and 1q32→q41, respectively, by fluorescence in situ hybridization". Genomics. ج. 23 ع. 3: 691–3. DOI:10.1006/geno.1994.1558. PMID:7851898.
^ "Entrez Gene: CENPF centromere protein F, 350/400ka (mitosin)". مؤرشف من الأصل في 2010-12-05.
^ Rattner JB، Rao A، Fritzler MJ، Valencia DW، Yen TJ (مارس 1994). "CENP-F is a .ca 400 kDa kinetochore protein that exhibits a cell-cycle dependent localization". Cell Motil Cytoskeleton. ج. 26 ع. 3: 214–26. DOI:10.1002/cm.970260305. PMID:7904902.

قراءة متعمقة

Ma L، Zhao X، Zhu X (2006). "Mitosin/CENP-F in mitosis, transcriptional control, and differentiation". J. Biomed. Sci. ج. 13 ع. 2: 205–13. DOI:10.1007/s11373-005-9057-3. PMID:16456711.
Liao H، Winkfein RJ، Mack G، وآخرون (1995). "CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis". J. Cell Biol. ج. 130 ع. 3: 507–18. DOI:10.1083/jcb.130.3.507. PMC:2120529. PMID:7542657.
Li Q، Ke Y، Kapp JA، وآخرون (1995). "A novel cell-cycle-dependent 350-kDa nuclear protein: C-terminal domain sufficient for nuclear localization". Biochem. Biophys. Res. Commun. ج. 212 ع. 1: 220–8. DOI:10.1006/bbrc.1995.1959. PMID:7612011.
Zhu X، Chang KH، He D، وآخرون (1995). "The C terminus of mitosin is essential for its nuclear localization, centromere/kinetochore targeting, and dimerization". J. Biol. Chem. ج. 270 ع. 33: 19545–50. DOI:10.1074/jbc.270.33.19545. PMID:7642639.
Zhu X، Mancini MA، Chang KH، وآخرون (1995). "Characterization of a novel 350-kilodalton nuclear phosphoprotein that is specifically involved in mitotic-phase progression". Mol. Cell. Biol. ج. 15 ع. 9: 5017–29. PMC:230749. PMID:7651420.
Li S، Ku CY، Farmer AA، وآخرون (1998). "Identification of a novel cytoplasmic protein that specifically binds to nuclear localization signal motifs". J. Biol. Chem. ج. 273 ع. 11: 6183–9. DOI:10.1074/jbc.273.11.6183. PMID:9497340.
Chan GK، Schaar BT، Yen TJ (1998). "Characterization of the kinetochore binding domain of CENP-E reveals interactions with the kinetochore proteins CENP-F and hBUBR1". J. Cell Biol. ج. 143 ع. 1: 49–63. DOI:10.1083/jcb.143.1.49. PMC:2132809. PMID:9763420.
Zhu X (1999). "Structural requirements and dynamics of mitosin-kinetochore interaction in M phase". Mol. Cell. Biol. ج. 19 ع. 2: 1016–24. PMC:116032. PMID:9891037.
Erlanson M، Casiano CA، Tan EM، وآخرون (1999). "Immunohistochemical analysis of the proliferation associated nuclear antigen CENP-F in non-Hodgkin's lymphoma". Mod. Pathol. ج. 12 ع. 1: 69–74. PMID:9950165.
Goodwin RL، Pabón-Peña LM، Foster GC، Bader D (1999). "The cloning and analysis of LEK1 identifies variations in the LEK/centromere protein F/mitosin gene family". J. Biol. Chem. ج. 274 ع. 26: 18597–604. DOI:10.1074/jbc.274.26.18597. PMID:10373470.
Ashar HR، James L، Gray K، وآخرون (2000). "Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules". J. Biol. Chem. ج. 275 ع. 39: 30451–7. DOI:10.1074/jbc.M003469200. PMID:10852915.
Kobayashi M، Hanai R (2001). "M phase-specific association of human topoisomerase IIIbeta with chromosomes". Biochem. Biophys. Res. Commun. ج. 287 ع. 1: 282–7. DOI:10.1006/bbrc.2001.5580. PMID:11549288.
Hussein D، Taylor SS (2003). "Farnesylation of Cenp-F is required for G2/M progression and degradation after mitosis". J. Cell Sci. ج. 115 ع. Pt 17: 3403–14. PMID:12154071.
Holstein SA، Hohl RJ (2003). "Synergistic interaction of lovastatin and paclitaxel in human cancer cells". Mol. Cancer Ther. ج. 1 ع. 2: 141–9. PMID:12467231.
Konstantinidou AE، Korkolopoulou P، Kavantzas N، وآخرون (2003). "Mitosin, a novel marker of cell proliferation and early recurrence in intracranial meningiomas". Histol. Histopathol. ج. 18 ع. 1: 67–74. PMID:12507285.
Yang ZY، Guo J، Li N، وآخرون (2004). "Mitosin/CENP-F is a conserved kinetochore protein subjected to cytoplasmic dynein-mediated poleward transport". Cell Res. ج. 13 ع. 4: 275–83. DOI:10.1038/sj.cr.7290172. PMID:12974617.
Laoukili J، Kooistra MR، Brás A، وآخرون (2005). "FoxM1 is required for execution of the mitotic programme and chromosome stability". Nat. Cell Biol. ج. 7 ع. 2: 126–36. DOI:10.1038/ncb1217. PMID:15654331.
Zhou X، Wang R، Fan L، وآخرون (2005). "Mitosin/CENP-F as a negative regulator of activating transcription factor-4". J. Biol. Chem. ج. 280 ع. 14: 13973–7. DOI:10.1074/jbc.M414310200. PMID:15677469.

هذه بذرة مقالة عن جين على كروموسوم 1 بحاجة للتوسيع. فضلًا شارك في تحريرها.

[1] Testa JR، Zhou JY، Bell DW، Yen TJ (مارس 1995). "Chromosomal localization of the genes encoding the kinetochore proteins CENPE and CENPF to human chromosomes 4q24→q25 and 1q32→q41, respectively, by fluorescence in situ hybridization". Genomics. ج. 23 ع. 3: 691–3. DOI:10.1006/geno.1994.1558. PMID:7851898.

[2] "Entrez Gene: CENPF centromere protein F, 350/400ka (mitosin)". مؤرشف من الأصل في 2010-12-05.

[3] Rattner JB، Rao A، Fritzler MJ، Valencia DW، Yen TJ (مارس 1994). "CENP-F is a .ca 400 kDa kinetochore protein that exhibits a cell-cycle dependent localization". Cell Motil Cytoskeleton. ج. 26 ع. 3: 214–26. DOI:10.1002/cm.970260305. PMID:7904902.

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