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Cytogenetic and genomic characterization of cell line ARH77

Cytogenetic and genomic characterization of cell line ARH77
Cytogenetic and genomic characterization of cell line ARH77
The cell line ARH77 is derived from a patient with plasma cell leukemia and has a complex and continually evolving karyotype. It is frequently used in biological studies of myeloma and plasma cell leukemia, so accurate characterization of the genome is valuable. Here we present a detailed cytogenetic investigation using G-banding and multicolor fluorescence in situ hybridization (M-FISH) in association with assessment of copy number alterations (CNAs) throughout the genome using array-based comparative genomic hybridization (aCGH). In addition to providing an accurate description of the karyotype, this complementary approach highlighted the relative merits of the individual techniques. Conventional cytogenetics and M-FISH indicated the location and types of the major chromosomal changes, whether balanced or unbalanced, and at the same time demonstrated the level of karyotypic evolution between cells. The aCGH profiles reflected the unbalanced chromosomal abnormalities detected by cytogenetics, providing refinement of their genomic breakpoint locations as well as the identification of novel genomic changes. Three aCGH platforms, comprising bacterial artificial chromosome (BAC) or oligonucleotide templates, were available for evaluation. Sixteen CNAs were consistently detected by all three platforms. Novel submicroscopic CNAs (similar to 0.4 Mb) were detected by the highest resolution platform only, whereas the clones from the BAC arrays provided locus-specific FISH probes for confirmation of CNA.
expression, DNA, multiple-myeloma, acute lymphoblastic-leukemia, tumors, identification, resolution, microarrays, cell, time, cells, leukemia, hybridization
0165-4608
40-45
Parker, Helen
33e0cd81-d45f-49bc-9539-09345d79d895
Cheung, Kan L.
c3e2bd17-d17f-4809-9c10-7e9dd19abc1d
Robinson, Hazel M.
c406aa02-ca17-4ba1-9aa4-24bab6415fc0
Harrison, Christine J.
52da7673-509c-4b88-b92e-0c021c9c7d3e
Strefford, Jon C.
3782b392-f080-42bf-bdca-8aa5d6ca532f
Parker, Helen
33e0cd81-d45f-49bc-9539-09345d79d895
Cheung, Kan L.
c3e2bd17-d17f-4809-9c10-7e9dd19abc1d
Robinson, Hazel M.
c406aa02-ca17-4ba1-9aa4-24bab6415fc0
Harrison, Christine J.
52da7673-509c-4b88-b92e-0c021c9c7d3e
Strefford, Jon C.
3782b392-f080-42bf-bdca-8aa5d6ca532f

Parker, Helen, Cheung, Kan L., Robinson, Hazel M., Harrison, Christine J. and Strefford, Jon C. (2008) Cytogenetic and genomic characterization of cell line ARH77. Cancer Genetics and Cytogenetics, 181 (1), 40-45. (doi:10.1016/j.cancergencyto.2007.10.013).

Record type: Article

Abstract

The cell line ARH77 is derived from a patient with plasma cell leukemia and has a complex and continually evolving karyotype. It is frequently used in biological studies of myeloma and plasma cell leukemia, so accurate characterization of the genome is valuable. Here we present a detailed cytogenetic investigation using G-banding and multicolor fluorescence in situ hybridization (M-FISH) in association with assessment of copy number alterations (CNAs) throughout the genome using array-based comparative genomic hybridization (aCGH). In addition to providing an accurate description of the karyotype, this complementary approach highlighted the relative merits of the individual techniques. Conventional cytogenetics and M-FISH indicated the location and types of the major chromosomal changes, whether balanced or unbalanced, and at the same time demonstrated the level of karyotypic evolution between cells. The aCGH profiles reflected the unbalanced chromosomal abnormalities detected by cytogenetics, providing refinement of their genomic breakpoint locations as well as the identification of novel genomic changes. Three aCGH platforms, comprising bacterial artificial chromosome (BAC) or oligonucleotide templates, were available for evaluation. Sixteen CNAs were consistently detected by all three platforms. Novel submicroscopic CNAs (similar to 0.4 Mb) were detected by the highest resolution platform only, whereas the clones from the BAC arrays provided locus-specific FISH probes for confirmation of CNA.

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More information

Published date: February 2008
Keywords: expression, DNA, multiple-myeloma, acute lymphoblastic-leukemia, tumors, identification, resolution, microarrays, cell, time, cells, leukemia, hybridization

Identifiers

Local EPrints ID: 62875
URI: http://eprints.soton.ac.uk/id/eprint/62875
ISSN: 0165-4608
PURE UUID: ec2fc62e-b23e-4a24-bb6b-a1ef8f848508
ORCID for Helen Parker: ORCID iD orcid.org/0000-0001-8308-9781
ORCID for Jon C. Strefford: ORCID iD orcid.org/0000-0002-0972-2881

Catalogue record

Date deposited: 04 Sep 2008
Last modified: 16 Mar 2024 03:40

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Contributors

Author: Helen Parker ORCID iD
Author: Kan L. Cheung
Author: Hazel M. Robinson
Author: Christine J. Harrison

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