@article{MTMT:1915157,
	title = {Characterization of the APC10/DOC1 subunit of the anaphase promoting complex in Drosophila melanogaster},
	url = {https://m2.mtmt.hu/api/publication/1915157},
	author = {Pál, Margit and Varga, Kata and Nagy, Olga Mária and Deák, Péter},
	doi = {10.1556/ABiol.58.2007.Suppl.5},
	journal-iso = {ACTA BIOL HUNG},
	journal = {ACTA BIOLOGICA HUNGARICA (1983-2018)},
	volume = {58},
	unique-id = {1915157},
	issn = {0236-5383},
	year = {2007},
	eissn = {1588-256X},
	pages = {51-64},
	orcid-numbers = {Nagy, Olga Mária/0000-0003-1471-5165}
}

@article{MTMT:1915149,
	title = {Structurally Related Tpr Subunits Contribute Differently to The Function of The Anaphase-promoting Complex in Drosophila Melanogaster},
	url = {https://m2.mtmt.hu/api/publication/1915149},
	author = {Pál, Margit and Nagy, Olga Mária and Ménesi, Dalma and Udvardy, Andor and Deák, Péter},
	doi = {10.1242/jcs.004762},
	journal-iso = {J CELL SCI},
	journal = {JOURNAL OF CELL SCIENCE},
	volume = {120},
	unique-id = {1915149},
	issn = {0021-9533},
	abstract = {The anaphase-promoting complex/cyclosome or APC/C is a key regulator of chromosome segregation and mitotic exit in eukaryotes. It contains at least 11 subunits, most of which are evolutionarily conserved. The most abundant constituents of the vertebrate APC/C are the four structurally related tetratrico-peptide repeat (TPR) subunits, the functions of which are not yet precisely understood. Orthologues of three of the TPR subunits have been identified in Drosophila. We have shown previously that one of the TPR subunits of the Drosophila APC/C, Apc3 (also known as Cdc27 or Makos), is essential for development, and perturbation of its function results in mitotic cyclin accumulation and metaphase-like arrest. In this study we demonstrate that the Drosophila APC/C associates with a new TPR protein, a genuine orthologue of the vertebrate Apc7 subunit that is not found in yeasts. In addition to this, transgenic flies knocked down for three of the TPR genes Apc6 (Cdc16), Apc7 and Apc8 (Cdc23), by RNA interference were established to investigate their function. Whole-body expression of subunit-specific dsRNA efficiently silences these genes resulting in only residual mRNA concentrations. Apc6/Cdc16 and Apc8/Cdc23 silencing induces developmental delay and causes different pupal lethality. Cytological examination showed that these animals had an elevated level of apoptosis, high mitotic index and delayed or blocked mitosis in a prometaphase-metaphase-like state with overcondensed chromosomes. The arrested neuroblasts contained elevated levels of cyclin B but, surprisingly, cyclin A appeared to be degraded normally. Contrary to the situation for the Apc6/Cdc16 and Apc8/Cdc23 genes, the apparent loss of Apc7 function does not lead to the above abnormalities. Instead, the Apc7 knocked down animals and null mutants are viable and fertile, although they display mild chromosome segregation defects and anaphase delay. Nevertheless, the Apc7 subunit shows synergistic genetic interaction with Apc8/Cdc23 that, together with the phenotypic data, assumes a limited functional role for Apc7. Taken together, these data suggest that the structurally related TPR subunits contribute differently to the function of the anaphase-promoting complex.},
	year = {2007},
	eissn = {1477-9137},
	pages = {3238-3248},
	orcid-numbers = {Nagy, Olga Mária/0000-0003-1471-5165}
}

@article{MTMT:1913542,
	title = {The E2-C vihar is required for the correct spatiotemporal proteolysis of cyclin B and itself undergoes cyclical degradation},
	url = {https://m2.mtmt.hu/api/publication/1913542},
	author = {Máthé, Endre and Kraft, C and Giet, F and Deák, Péter and Peters, JM and Glover, DM},
	doi = {10.1016/j.cub.2004.09.023},
	journal-iso = {CURR BIOL},
	journal = {CURRENT BIOLOGY},
	volume = {14},
	unique-id = {1913542},
	issn = {0960-9822},
	year = {2004},
	eissn = {1879-0445},
	pages = {1723-1733}
}

@article{MTMT:1912970,
	title = {The arabidopsis anaphase-promoting complex or cyclosome: molecular and genetic characterization of the APC2 subunit},
	url = {https://m2.mtmt.hu/api/publication/1912970},
	author = {Capron, A and Serralbo, O and Fülöp, Katalin and Frugier, F and Parmentier, Y and Dong, AW and Lecureuil, A and Guerche, P and Kondorosi, Éva and Scheres, B and Genschik, P},
	doi = {10.1105/tpc.013847},
	journal-iso = {PLANT CELL},
	journal = {PLANT CELL},
	volume = {15},
	unique-id = {1912970},
	issn = {1040-4651},
	year = {2003},
	eissn = {1532-298X},
	pages = {2370-2382},
	orcid-numbers = {Kondorosi, Éva/0000-0002-4065-8515}
}

@article{MTMT:1912977,
	title = {Mutations in makos, a Drosophila gene encoding the Cdc27 subunit of the anaphase promoting complex, enhance centrosomal defects in polo and are suppressed by mutations in twins/aar, which encodes a regulatory subunit of PP2A},
	url = {https://m2.mtmt.hu/api/publication/1912977},
	author = {Deák, Péter and Donaldson, M and Glover, DM},
	doi = {10.1242/jcs.00722},
	journal-iso = {J CELL SCI},
	journal = {JOURNAL OF CELL SCIENCE},
	volume = {116},
	unique-id = {1912977},
	issn = {0021-9533},
	year = {2003},
	eissn = {1477-9137},
	pages = {4147-4158}
}