BÁRTOVÁ, Eva, Andrea HARNIČAROVÁ, Jana KREJČÍ, Luděk STRAŠÁK a Stanislav KOZUBEK. Single-cell c-myc gene expression in relationship to nuclear domains. Chromosome Research. Dordrecht: Kluwer Academic Publishers, 2008, roč. 16, č. 2, s. 325-343. ISSN 0967-3849.
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Základní údaje
Originální název Single-cell c-myc gene expression in relationship to nuclear domains.
Název česky Exprese c-myc ve vztahu k jaderným doménám
Autoři BÁRTOVÁ, Eva (203 Česká republika), Andrea HARNIČAROVÁ (703 Slovensko, garant), Jana KREJČÍ (203 Česká republika), Luděk STRAŠÁK (203 Česká republika) a Stanislav KOZUBEK (203 Česká republika).
Vydání Chromosome Research, Dordrecht, Kluwer Academic Publishers, 2008, 0967-3849.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor Genetika a molekulární biologie
Stát vydavatele Česká republika
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 3.405
Kód RIV RIV/00216224:14110/08:00024465
Organizační jednotka Lékařská fakulta
UT WoS 000253753800009
Klíčová slova anglicky c-myc gene; nuclear speckles; nucleolus; promyelocytic leukaemia body;transcription site
Štítky c-myc gene, nuclear speckles, nucleolus, promyelocytic leukaemia body, transcription site
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Gabriela Petrovičová, učo 239322. Změněno: 17. 6. 2009 17:09.
Anotace
Nuclear locations of the c-myc gene and its transcripts (c-myc (T)) have been investigated in relation to nuclear domains involved in RNA synthesis and processing. Transcription of the c-myc gene appears to be linked to the late G(1)- and preferentially to S-phases of the cell cycle. The c-myc gene and its transcripts were positioned non-randomly within the interphase nucleus; additionally, c-myc RNA signals accumulated at nucleoli. Using oligo-probes, designed to exon II and exon III of the c-myc gene, single c-myc (T) was preferentially observed in human carcinoma HT29 and A549 cells. Conversely, human embryonal teratocarcinoma NTERA cells were characterized by the presence of multiple c-myc RNA signals located in both the nucleoli and nucleoplasm. When accumulated at nucleoli, c-myc (T) occupied the periphery of this organelle, though not those associated with the cultivation surface. In HT29 cells, approximately 80% of c-myc (T) co-localized with the RNAP II positive regions, so-called transcription factories. However, in approximately 20% of the cells with c-myc transcripts, the c-myc (T) was released from the site of synthesis, and was not associated with either transcription factories or SC35 domains. In approximately 60% of nuclei with c-myc (T), these signals were located in close proximity to the SC35 regions, but promyelocytic leukaemia bodies were associated with c-myc (T) only in approximately 20% of the nuclei. Taken together, c-myc RNA signals were positioned in the most internal parts of the cell nuclei preferentially associated with the nucleoli. Specific nuclear and nucleolar positioning probably reflects the kinetics of c-myc RNA metabolism.
Anotace česky
Článek se zabývá studiem exprese c-myc genu.
VytisknoutZobrazeno: 10. 7. 2024 15:17