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Ig gene diversification and selection in follicular lymphoma, diffuse large B cell lymphoma and primary central nervous system lymphoma revealed by lineage tree and mutation analyses

Ig gene diversification and selection in follicular lymphoma, diffuse large B cell lymphoma and primary central nervous system lymphoma revealed by lineage tree and mutation analyses
Ig gene diversification and selection in follicular lymphoma, diffuse large B cell lymphoma and primary central nervous system lymphoma revealed by lineage tree and mutation analyses
Follicular lymphoma (FL), diffuse large B cell lymphoma (DLBCL) and primary central nervous system lymphoma are B cell malignancies. FL and DLBCL have a germinal center origin. We have applied mutational analyses and a novel algorithm for quantifying shape properties of mutational lineage trees to investigate the nature of the diversification, somatic hypermutation and selection processes that affect B cell clones in these malignancies and reveal whether they differ from normal responses. Lineage tree analysis demonstrated higher diversification and mutations per cell in the lymphoma clones. This was caused solely by the longer diversification times of the malignant clones, as their recent diversification processes were similar to those of normal responses, implying similar mutation frequencies. Since previous analyses of antigen-driven selection were shown to yield false positives, we performed a corrected analysis of replacement and silent mutation patterns, which revealed selection against replacement mutations in the framework regions, responsible for the structural integrity of the B cell receptor, but not for positive selection for replacements in the complementary determining regions. Most replacements, however, were neutral or conservative, suggesting that if at all selection operates in these malignancies it is for structural B cell receptor integrity but not for antigen binding.
germinal center, ig genes, lineage trees, lymphomas
0953-8178
875-887
Zuckerman, Neta S.
5f96dd03-480c-450c-bbc1-d64c6a57593d
McCann, Katy J.
154f6b6d-c8b2-43b2-a8a9-ffe243da40c6
Ottensmeier, Christian H.
42b8a398-baac-4843-a3d6-056225675797
Barak, Michal
74951550-4080-4038-a062-d4ec3dc665a9
Shahaf, Gitit
3ddd2487-0117-492f-8eb6-2850566fe815
Edelman, Hanna
093142bf-813f-4bf8-be17-c84eb61c87a1
Dunn-Walters, Deborah
bb0710ba-e622-4f22-98ea-cfa73b386f02
Abraham, Roshini S.
1744a446-98a6-4130-ac92-1b203e3c6129
Stevenson, Freda K.
ba803747-c0ac-409f-a9c2-b61fde009f8c
Mehr, Ramit
f5d56f11-71bc-4801-8d25-f0f156b8001d
Zuckerman, Neta S.
5f96dd03-480c-450c-bbc1-d64c6a57593d
McCann, Katy J.
154f6b6d-c8b2-43b2-a8a9-ffe243da40c6
Ottensmeier, Christian H.
42b8a398-baac-4843-a3d6-056225675797
Barak, Michal
74951550-4080-4038-a062-d4ec3dc665a9
Shahaf, Gitit
3ddd2487-0117-492f-8eb6-2850566fe815
Edelman, Hanna
093142bf-813f-4bf8-be17-c84eb61c87a1
Dunn-Walters, Deborah
bb0710ba-e622-4f22-98ea-cfa73b386f02
Abraham, Roshini S.
1744a446-98a6-4130-ac92-1b203e3c6129
Stevenson, Freda K.
ba803747-c0ac-409f-a9c2-b61fde009f8c
Mehr, Ramit
f5d56f11-71bc-4801-8d25-f0f156b8001d

Zuckerman, Neta S., McCann, Katy J., Ottensmeier, Christian H., Barak, Michal, Shahaf, Gitit, Edelman, Hanna, Dunn-Walters, Deborah, Abraham, Roshini S., Stevenson, Freda K. and Mehr, Ramit (2010) Ig gene diversification and selection in follicular lymphoma, diffuse large B cell lymphoma and primary central nervous system lymphoma revealed by lineage tree and mutation analyses. International Immunology, 22 (11), 875-887. (doi:10.1093/intimm/dxq441). (PMID:21059768)

Record type: Article

Abstract

Follicular lymphoma (FL), diffuse large B cell lymphoma (DLBCL) and primary central nervous system lymphoma are B cell malignancies. FL and DLBCL have a germinal center origin. We have applied mutational analyses and a novel algorithm for quantifying shape properties of mutational lineage trees to investigate the nature of the diversification, somatic hypermutation and selection processes that affect B cell clones in these malignancies and reveal whether they differ from normal responses. Lineage tree analysis demonstrated higher diversification and mutations per cell in the lymphoma clones. This was caused solely by the longer diversification times of the malignant clones, as their recent diversification processes were similar to those of normal responses, implying similar mutation frequencies. Since previous analyses of antigen-driven selection were shown to yield false positives, we performed a corrected analysis of replacement and silent mutation patterns, which revealed selection against replacement mutations in the framework regions, responsible for the structural integrity of the B cell receptor, but not for positive selection for replacements in the complementary determining regions. Most replacements, however, were neutral or conservative, suggesting that if at all selection operates in these malignancies it is for structural B cell receptor integrity but not for antigen binding.

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More information

Published date: 8 November 2010
Keywords: germinal center, ig genes, lineage trees, lymphomas

Identifiers

Local EPrints ID: 179121
URI: http://eprints.soton.ac.uk/id/eprint/179121
ISSN: 0953-8178
PURE UUID: 84cee5b1-f7a1-46a9-894c-f56f022ebaa5
ORCID for Freda K. Stevenson: ORCID iD orcid.org/0000-0002-0933-5021

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Date deposited: 31 Mar 2011 11:40
Last modified: 15 Mar 2024 02:53

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Contributors

Author: Neta S. Zuckerman
Author: Katy J. McCann
Author: Michal Barak
Author: Gitit Shahaf
Author: Hanna Edelman
Author: Deborah Dunn-Walters
Author: Roshini S. Abraham
Author: Ramit Mehr

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