Distinct Patterns of Colocalization of the CCND1 and CMYC Genes With Their Potential Translocation Partner IGH at Successive Stages of B‐Cell Differentiation. Issue 7 (6th March 2016)
- Record Type:
- Journal Article
- Title:
- Distinct Patterns of Colocalization of the CCND1 and CMYC Genes With Their Potential Translocation Partner IGH at Successive Stages of B‐Cell Differentiation. Issue 7 (6th March 2016)
- Main Title:
- Distinct Patterns of Colocalization of the CCND1 and CMYC Genes With Their Potential Translocation Partner IGH at Successive Stages of B‐Cell Differentiation
- Authors:
- Sklyar, Ilya
Iarovaia, Olga V.
Gavrilov, Alexey A.
Pichugin, Andrey
Germini, Diego
Tsfasman, Tatiana
Caron, Gersende
Fest, Thierry
Lipinski, Marc
Razin, Sergey V.
Vassetzky, Yegor S. - Abstract:
- ABSTRACT: The immunoglobulin heavy chain ( IGH ) locus is submitted to intra‐chromosomal DNA breakages and rearrangements during normal B cell differentiation that create a risk for illegitimate inter‐chromosomal translocations leading to a variety of B‐cell malignancies. In most Burkitt's and Mantle Cell lymphomas, specific chromosomal translocations juxtapose the IGH locus with a CMYC or Cyclin D1 ( CCND1 ) gene, respectively. 3D‐fluorescence in situ hybridization was performed on normal peripheral B lymphocytes induced to mature in vitro from a naive state to the stage where they undergo somatic hypermutation (SHM) and class switch recombination (CSR). The CCND1 genes were found very close to the IGH locus in naive B cells and further away after maturation. In contrast, the CMYC alleles became localized closer to an IGH locus at the stage of SHM/CSR. The colocalization observed between the two oncogenes and the IGH locus at successive stages of B‐cell differentiation occurred in the immediate vicinity of the nucleolus, consistent with the known localization of the RAGs and AID enzymes whose function has been demonstrated in IGH physiological rearrangements. We propose that the chromosomal events leading to Mantle Cell lymphoma and Burkitt's lymphoma are favored by the colocalization of CCND1 and CMYC with IGH at the time the concerned B cells undergo VDJ recombination or SHM/CSR, respectively. J. Cell. Biochem. 117: 1506–1510, 2016. © 2016 Wiley Periodicals, Inc. AbstractABSTRACT: The immunoglobulin heavy chain ( IGH ) locus is submitted to intra‐chromosomal DNA breakages and rearrangements during normal B cell differentiation that create a risk for illegitimate inter‐chromosomal translocations leading to a variety of B‐cell malignancies. In most Burkitt's and Mantle Cell lymphomas, specific chromosomal translocations juxtapose the IGH locus with a CMYC or Cyclin D1 ( CCND1 ) gene, respectively. 3D‐fluorescence in situ hybridization was performed on normal peripheral B lymphocytes induced to mature in vitro from a naive state to the stage where they undergo somatic hypermutation (SHM) and class switch recombination (CSR). The CCND1 genes were found very close to the IGH locus in naive B cells and further away after maturation. In contrast, the CMYC alleles became localized closer to an IGH locus at the stage of SHM/CSR. The colocalization observed between the two oncogenes and the IGH locus at successive stages of B‐cell differentiation occurred in the immediate vicinity of the nucleolus, consistent with the known localization of the RAGs and AID enzymes whose function has been demonstrated in IGH physiological rearrangements. We propose that the chromosomal events leading to Mantle Cell lymphoma and Burkitt's lymphoma are favored by the colocalization of CCND1 and CMYC with IGH at the time the concerned B cells undergo VDJ recombination or SHM/CSR, respectively. J. Cell. Biochem. 117: 1506–1510, 2016. © 2016 Wiley Periodicals, Inc. Abstract : Burkitt's and Mantle Cell lymphomas, specific chromosomal translocations juxtapose the IGH locus with a CMYC or Cyclin D1 ( CCND1 ) gene. We propose that the chromosomal events leading to Mantle Cell lymphoma and Burkitt's lymphoma are favored by the colocalization of CCND1 and CMYC with IGH at the time the concerned B cells undergo VDJ recombination or SHM/CSR, respectively. … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 117:Issue 7(2016:Jul.)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 117:Issue 7(2016:Jul.)
- Issue Display:
- Volume 117, Issue 7 (2016)
- Year:
- 2016
- Volume:
- 117
- Issue:
- 7
- Issue Sort Value:
- 2016-0117-0007-0000
- Page Start:
- 1506
- Page End:
- 1510
- Publication Date:
- 2016-03-06
- Subjects:
- NUCLEAR ORGANIZATION -- B‐CELL LYMPHOMA -- ILLEGITIMATE RECOMBINATION -- IGH -- CMYC -- CCND1
Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.25516 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
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- 2070.xml