Nuclear topography of beta-like globin gene cluster in
IL-3-stimulated human leukemic K-562 cells

J 2004

Nuclear topography of beta-like globin gene cluster in IL-3-stimulated human leukemic K-562 cells

GALIOVÁ, Gabriela, Eva BÁRTOVÁ a Stanislav KOZUBEK

Základní údaje

Originální název

Nuclear topography of beta-like globin gene cluster in IL-3-stimulated human leukemic K-562 cells

Autoři

GALIOVÁ, Gabriela, Eva BÁRTOVÁ a Stanislav KOZUBEK

Vydání

Blood Cells, Molecules and Diseases, Orlando, Florida, Academic Press, 2004, 1079-9796

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

Genetika a molekulární biologie

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 2.549

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000222730500002

Klíčová slova anglicky

beta-like globin gene cluster; K-562 cells; nuclear topography; gene activity

Štítky

beta-like globin gene cluster, gene activity, K-562 cells, Nuclear topography

Změněno: 14. 1. 2005 14:41, prof. RNDr. Michal Kozubek, Ph.D.

Anotace

V originále

The beta-like globin genes epsilon, Ggamma, Agamma, delta and beta, forming specific clusters on chromosome 11, are transcriptionally regulated by the locus control region (LCR). The members of beta-like globin gene cluster (11p15.4) are variously switched during ontogenetic dependent erythropoiesis; however, changes of globin gene expression can be also observed during erythroid differentiation of bone marrow cells. In our experiments, interleukin-3 (IL-3)-stimulated human leukemic K-562 cells were used as a model system in which nuclear organization and expression of the beta-like globin gene cluster was investigated. In addition, the influence of IL-3 on the arrangement of chromosome 11 territory was analyzed. We observed that the beta-globin gene is not expressed in progenitor (nondifferentiated) K-562 cells, but is, however, activated after IL-3 stimulation of the K-562 population. A similar nuclear location of beta-like globin gene clusters was found in both control and IL-3-treated cells, which indicates that changes in cluster gene expression are accompanied by conserved nuclear topography of the gene cluster studied. On the other hand, the studied type of cell differentiation was characterized by relocation of chromosome 11 and its centromeric regions closer to the nuclear periphery, which seems to be a general feature of many pathways of cellular maturation. The beta-like globin gene cluster was observed on chromatin loops extended away from compact chromosome 11 territories that were more condensed in regions closer to the nuclear membrane. The relocation of chromosome 11 territories towards the nuclear periphery and simultaneous appearance of chromatin loops may explain the conserved nuclear positioning of the gene cluster studied.

Citovat

GALIOVÁ, Gabriela, Eva BÁRTOVÁ a Stanislav KOZUBEK. Nuclear topography of beta-like globin gene cluster in IL-3-stimulated human leukemic K-562 cells. Blood Cells, Molecules and Diseases. Orlando, Florida: Academic Press, 2004, roč. 33, č. 1, s. 4-14. ISSN 1079-9796.

@article{564367,
   author = {Galiová, Gabriela and Bártová, Eva and Kozubek, Stanislav},
   article_location = {Orlando, Florida},
   article_number = {1},
   keywords = {beta-like globin gene cluster; K-562 cells; nuclear topography; gene activity},
   language = {eng},
   issn = {1079-9796},
   journal = {Blood Cells, Molecules and Diseases},
   title = {Nuclear topography of beta-like globin gene cluster in IL-3-stimulated human leukemic K-562 cells},
   volume = {33},
   year = {2004}
}

TY  - JOUR
ID  - 564367
AU  - Galiová, Gabriela - Bártová, Eva - Kozubek, Stanislav
PY  - 2004
TI  - Nuclear topography of beta-like globin gene cluster in IL-3-stimulated human leukemic K-562 cells
JF  - Blood Cells, Molecules and Diseases
VL  - 33
IS  - 1
SP  - 4-14
EP  - 4-14
PB  - Academic Press
SN  - 10799796
KW  - beta-like globin gene cluster
KW  - K-562 cells
KW  - nuclear topography
KW  - gene activity
N2  - The beta-like globin genes epsilon, Ggamma, Agamma, delta and beta, forming specific clusters on chromosome 11, are transcriptionally regulated by the locus control region (LCR). The members of beta-like globin gene cluster (11p15.4) are variously switched during ontogenetic dependent erythropoiesis; however, changes of globin gene expression can be also observed during erythroid differentiation of bone marrow cells. In our experiments, interleukin-3 (IL-3)-stimulated human leukemic K-562 cells were used as a model system in which nuclear organization and expression of the beta-like globin gene cluster was investigated. In addition, the influence of IL-3 on the arrangement of chromosome 11 territory was analyzed. We observed that the beta-globin gene is not expressed in progenitor (nondifferentiated) K-562 cells, but is, however, activated after IL-3 stimulation of the K-562 population. A similar nuclear location of beta-like globin gene clusters was found in both control and IL-3-treated cells, which indicates that changes in cluster gene expression are accompanied by conserved nuclear topography of the gene cluster studied. On the other hand, the studied type of cell differentiation was characterized by relocation of chromosome 11 and its centromeric regions closer to the nuclear periphery, which seems to be a general feature of many pathways of cellular maturation. The beta-like globin gene cluster was observed on chromatin loops extended away from compact chromosome 11 territories that were more condensed in regions closer to the nuclear membrane. The relocation of chromosome 11 territories towards the nuclear periphery and simultaneous appearance of chromatin loops may explain the conserved nuclear positioning of the gene cluster studied.
ER  -

GALIOVÁ, Gabriela, Eva BÁRTOVÁ a Stanislav KOZUBEK. Nuclear topography of beta-like globin gene cluster in IL-3-stimulated human leukemic K-562 cells. \textit{Blood Cells, Molecules and Diseases}. Orlando, Florida: Academic Press, 2004, roč.~33, č.~1, s.~4-14. ISSN~1079-9796.

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