FALK, Martin, Emilie LUKÁŠOVÁ, Mario FARETTA, Ivan DELLINO, Stanislav KOZUBEK, Giuseppe PELICCI, Michal KOZUBEK and Mariano ROCHI. Colocalization of PML bodies and PML/RARalpha microspeckles with up- and down-regulated loci and changes of chromatin structure in APL leukemia cells. In Biophysics of the Genome. First Edition 2004. Brno: Masaryk University, 2004, p. 8-23. ISBN 80-210-3560-9.
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Basic information
Original name Colocalization of PML bodies and PML/RARalpha microspeckles with up- and down-regulated loci and changes of chromatin structure in APL leukemia cells
Name in Czech Kolokalizace PML tělísek a PML/RARalpha mikroshluků s up- a down- regulovanými lokusy a změny struktury chromatinu u APL leukemických buněk
Authors FALK, Martin (203 Czech Republic), Emilie LUKÁŠOVÁ (203 Czech Republic), Mario FARETTA (380 Italy), Ivan DELLINO (380 Italy), Stanislav KOZUBEK (203 Czech Republic, guarantor), Giuseppe PELICCI (380 Italy), Michal KOZUBEK (203 Czech Republic) and Mariano ROCHI (380 Italy).
Edition First Edition 2004. Brno, Biophysics of the Genome, p. 8-23, 16 pp. 2004.
Publisher Masaryk University
Other information
Original language English
Type of outcome Proceedings paper
Field of Study Genetics and molecular biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14330/04:00009698
Organization unit Faculty of Informatics
ISBN 80-210-3560-9
Keywords in English Cytometry
Tags Cytometry
Tags International impact
Changed by Changed by: prof. RNDr. Michal Kozubek, Ph.D., učo 3740. Changed: 29/10/2010 14:36.
Abstract
The reciprocal translocation between PML and RARalpha genes associated with acute promyelocytic leukemia (APL) results in disintegration of PML bodies and expression of the fusion protein PML/RARalpha in transformed APL cells. Transcription intensity of particular genes were compared between Zn-treated (APL) and untreated (healthy) U937 PIR9 cells, stably transfected by the expression vector carrying the PML/RARalpha fusion gene under the control of Zn-inducible promoter; downregulation of many genes clustered in the locus 19p13.3 and upregulation of some of those in Xq28-Xqter were revealed by microchip analysis and RT-PCR after zinc treatment. We have examined the colocalization of these up- (Xq28-qter)-regulated (19p13.3)chromosomal loci with PML bodies in normal and PML/RARalpha microspeckles in transformed APL cells respectively, as well as the changes in chromatin structure of these loci induced in APL cells by PML/RARalpha-altered transcription. Most frequently, colocalization or very close proximity (< PML body diameter) of the one of two homologous loci was observed for loci 19p13.3 (more than 50%) and Xq28-Xqter (25-35%), contrary to the control locus 13q22.3 (containing none clusters of PML/RARalpha-regulated genes) where colocalization was found in only 5-6%. On the other hand, both homologous loci 19p13.3 usually colocalized with PML/RARalpha microspeckles (more than 70% of nuclei) after disintegration of PML bodies in zinc treated PIR9 cells (APL cells). After all-trans retinoic acid (ATRA) treatment of APL cells, reconstituted PML bodies and colocalization frequencies resembling those in normal cells reappeared. Conversely, frequency of colocalizing loci 13q22.3 and Xq28-Xqter remained very similar in normal, APL and ATRA-treated APL cells. The degree of chromatin compaction was evaluated according to the mutual 3D distances between the pairs of DNA probes separated by short molecular distances (1.5-4 Mbp), for the first time in natural DNA sequences. The distances between the probes in the down-regulated region 19p13.3 were significantly shortened (about 15-20%) in APL cells, whereas remained similar for the cen17-17q11.2 (control) and Xq28-Xqter (upregulated)loci. After ATRA treatment the level of chromatin condensation in 19p13.3 locus reverted to original values in normal cells. These results together with the observed high colocalization frequency of PML/RARalpha with the downregulated locus 19p13.3 support the mechanistic model of gene silencing in APL, where binding of PML/RARalpha to the particular loci results in strong attraction of HDACs, consequent histone deacethylation, chromatin condensation and gene silencing. Not conclusive rule of proportion between transcription intensity and chromatin condensation together with unchanged radial distances of loci (nuclear center-to-locus distances) after their activation/silencing however indicate that the higher-order chromatin structure is not necessarily influenced by transcription process. On the other hand, upregulation of PML/RARalpha- activated genes is obviously not caused by direct PML/RARalpha binding to their DNA sequences.
Abstract (in Czech)
Kolokalizace PML tělísek a PML/RARalpha mikroshluků s up- a down- regulovanými lokusy a změny struktury chromatinu u APL leukemických buněk.
Links
GA202/02/0804, research and development projectName: Určení radiačního rizika pro vznik chronické myeloidní leukémie na základě měření vzdáleností mezi geny ABL a BCR v hematopoietických buňkách
Investor: Czech Science Foundation, Chronic myeloid leukemia radiation risk estimation based on BCR-ABL distances in hemotopoietic cells
IAA1065203, research and development projectName: Využití kombinace laserových mikrosvazkových a cytometrických technik ke studiu struktury a dynamiky lidského genomu
Investor: Academy of Sciences of the Czech Republic, The use of combination of laser microbeam and cytometric techniques in the study of the structure and dynamics of human genome
IAA5004306, research and development projectName: Struktura lidského genomu
Investor: Academy of Sciences of the Czech Republic, Human genome structure
IBS5004010, research and development projectName: Vývoj nových diagnostických technik pro onkologii
Investor: Academy of Sciences of the Czech Republic, Development of new diagnostic teniques for oncology
ME 565, research and development projectName: Struktura a funkce interfázních chromosomů
NC6987, research and development projectName: Epigeneticky kontrolované změny exprese genů u nádorových onemocnění
Investor: Ministry of Health of the CR, Epigenetic control of gene expression in malignant diseases
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