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. 1995 Jan;146(1):46–55.

Analysis of T cell receptor-gamma gene rearrangements by denaturing gradient gel electrophoresis of GC-clamped polymerase chain reaction products. Correlation with tumor-specific sequences.

T C Greiner 1, M Raffeld 1, C Lutz 1, F Dick 1, E S Jaffe 1
PMCID: PMC1870776  PMID: 7856738

Abstract

We describe a modified denaturing gradient gel electrophoresis (DGGE) procedure with a 40-nucleotide GC clamp in the polymerase chain reaction to improve resolution in amplifying T cell receptor-gamma (TCR-gamma) rearrangements. DNA from 46 cases of lymphoblastic leukemia/lymphoma, 5T cell lines, 2 B cell lines, 7 normal lymphocytes, and 3 cases of Hodgkin's disease was amplified by polymerase chain reaction. In addition, 20 cases of paraffin-embedded T cell lymphomas and 5 cases of reactive hyperplasia were also studied. Clonal TCR-gamma rearrangements were identified on DGGE by the presence of a predominant band. Results obtained from 5 T cell lines and 12 lymphoblastic leukemia/lymphomas containing known TCR-gamma gene rearrangements revealed 100% concordance in detecting clonal rearrangements between DGGE and traditional Southern blot analysis. Of the remaining 34 lymphoblastic leukemia/lymphoma cases studied by DGGE alone, 30 were positive. DGGE analysis of 10 lymphoblastic leukemia/lymphoma cases with known group IV gamma to J gamma 1 or J gamma 2 rearrangement sequences confirmed that the electrophoretic migration was dependent on the tumor-specific rearranged TCR-gamma sequence. In addition, 17 of 20 cases of paraffin-embedded T cell lymphomas were positive by DGGE, 6 of which had the clonal population also identified in fresh tissue DNA. DGGE analysis of GC-clamped polymerase chain reaction products can provide a way to more accurately detect TCR-gamma clonality of lymphoid tumors and can be applied to archival tissues.

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Selected References

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  1. Abrams E. S., Murdaugh S. E., Lerman L. S. Comprehensive detection of single base changes in human genomic DNA using denaturing gradient gel electrophoresis and a GC clamp. Genomics. 1990 Aug;7(4):463–475. doi: 10.1016/0888-7543(90)90188-z. [DOI] [PubMed] [Google Scholar]
  2. Bahler D. W., Berry G., Oksenberg J., Warnke R. A., Levy R. Diversity of T-cell antigen receptor variable genes used by mycosis fungoides cells. Am J Pathol. 1992 Jan;140(1):1–8. [PMC free article] [PubMed] [Google Scholar]
  3. Bourguin A., Tung R., Galili N., Sklar J. Rapid, nonradioactive detection of clonal T-cell receptor gene rearrangements in lymphoid neoplasms. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8536–8540. doi: 10.1073/pnas.87.21.8536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Forster A., Huck S., Ghanem N., Lefranc M. P., Rabbitts T. H. New subgroups in the human T cell rearranging V gamma gene locus. EMBO J. 1987 Jul;6(7):1945–1950. doi: 10.1002/j.1460-2075.1987.tb02456.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Goudie R. B., Karim S. N., Mills K., Alcorn M., Lee F. D. A sensitive method of screening for dominant T cell clones by amplification of T cell gamma gene rearrangements with the polymerase chain reaction. J Pathol. 1990 Nov;162(3):191–196. doi: 10.1002/path.1711620304. [DOI] [PubMed] [Google Scholar]
  6. Hansen-Hagge T. E., Yokota S., Bartram C. R. Detection of minimal residual disease in acute lymphoblastic leukemia by in vitro amplification of rearranged T-cell receptor delta chain sequences. Blood. 1989 Oct;74(5):1762–1767. [PubMed] [Google Scholar]
  7. Heller M. J., Burgart L. J., TenEyck C. J., Anderson M. E., Greiner T. C., Robinson R. A. An efficient method for the extraction of DNA from formalin-fixed, paraffin-embedded tissue by sonication. Biotechniques. 1991 Sep;11(3):372-4, 376-7. [PubMed] [Google Scholar]
  8. Huck S., Lefranc M. P. Rearrangements to the JP1, JP and JP2 segments in the human T-cell rearranging gamma gene (TRG gamma) locus. FEBS Lett. 1987 Nov 30;224(2):291–296. doi: 10.1016/0014-5793(87)80472-6. [DOI] [PubMed] [Google Scholar]
  9. Imrie F., Karim S. N., Goudie R. B. Error in reported frequency of dominant T-cell receptor V gamma 8 gene rearrangements in T-cell lymphomas. J Pathol. 1992 Apr;166(4):417–418. doi: 10.1002/path.1711660416. [DOI] [PubMed] [Google Scholar]
  10. Knowles D. M. Immunophenotypic and antigen receptor gene rearrangement analysis in T cell neoplasia. Am J Pathol. 1989 Apr;134(4):761–785. [PMC free article] [PubMed] [Google Scholar]
  11. LeFranc M. P., Forster A., Baer R., Stinson M. A., Rabbitts T. H. Diversity and rearrangement of the human T cell rearranging gamma genes: nine germ-line variable genes belonging to two subgroups. Cell. 1986 Apr 25;45(2):237–246. doi: 10.1016/0092-8674(86)90388-0. [DOI] [PubMed] [Google Scholar]
  12. Lefranc M. P., Forster A., Rabbitts T. H. Rearrangement of two distinct T-cell gamma-chain variable-region genes in human DNA. 1986 Jan 30-Feb 5Nature. 319(6052):420–422. doi: 10.1038/319420a0. [DOI] [PubMed] [Google Scholar]
  13. Lorenzen J., Jux G., Zhao-Höhn M., Klöckner A., Fischer R., Hansmann M. L. Detection of T-cell clonality in paraffin-embedded tissues. Diagn Mol Pathol. 1994 Jun;3(2):93–99. doi: 10.1097/00019606-199406000-00005. [DOI] [PubMed] [Google Scholar]
  14. Lutz C. T., Galles M. E., Kemp J. D., Goeken J. A., Dick F. R. Kappa immunoglobulin light chain gene rearrangement in a T-lineage chronic lymphocytic leukemia. Am J Clin Pathol. 1990 May;93(5):702–705. doi: 10.1093/ajcp/93.5.702. [DOI] [PubMed] [Google Scholar]
  15. Macintyre E. A., d'Auriol L., Duparc N., Leverger G., Galibert F., Sigaux F. Use of oligonucleotide probes directed against T cell antigen receptor gamma delta variable-(diversity)-joining junctional sequences as a general method for detecting minimal residual disease in acute lymphoblastic leukemias. J Clin Invest. 1990 Dec;86(6):2125–2135. doi: 10.1172/JCI114951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. McCarthy K. P., Sloane J. P., Kabarowski J. H., Matutes E., Wiedemann L. M. A simplified method of detection of clonal rearrangements of the T-cell receptor-gamma chain gene. Diagn Mol Pathol. 1992 Sep;1(3):173–179. [PubMed] [Google Scholar]
  17. McCarthy K. P., Sloane J. P., Kabarowski J. H., Matutes E., Wiedemann L. M. The rapid detection of clonal T-cell proliferations in patients with lymphoid disorders. Am J Pathol. 1991 Apr;138(4):821–828. [PMC free article] [PubMed] [Google Scholar]
  18. Myers R. M., Maniatis T., Lerman L. S. Detection and localization of single base changes by denaturing gradient gel electrophoresis. Methods Enzymol. 1987;155:501–527. doi: 10.1016/0076-6879(87)55033-9. [DOI] [PubMed] [Google Scholar]
  19. Neale G. A., Menarguez J., Kitchingman G. R., Fitzgerald T. J., Koehler M., Mirro J., Jr, Goorha R. M. Detection of minimal residual disease in T-cell acute lymphoblastic leukemia using polymerase chain reaction predicts impending relapse. Blood. 1991 Aug 1;78(3):739–747. [PubMed] [Google Scholar]
  20. Orita M., Suzuki Y., Sekiya T., Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics. 1989 Nov;5(4):874–879. doi: 10.1016/0888-7543(89)90129-8. [DOI] [PubMed] [Google Scholar]
  21. Saiki R. K., Gelfand D. H., Stoffel S., Scharf S. J., Higuchi R., Horn G. T., Mullis K. B., Erlich H. A. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988 Jan 29;239(4839):487–491. doi: 10.1126/science.2448875. [DOI] [PubMed] [Google Scholar]
  22. Sheffield V. C., Cox D. R., Lerman L. S., Myers R. M. Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes. Proc Natl Acad Sci U S A. 1989 Jan;86(1):232–236. doi: 10.1073/pnas.86.1.232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sheffield V. C., Fishman G. A., Beck J. S., Kimura A. E., Stone E. M. Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis. Am J Hum Genet. 1991 Oct;49(4):699–706. [PMC free article] [PubMed] [Google Scholar]
  24. Slack D. N., McCarthy K. P., Wiedemann L. M., Sloane J. P. Evaluation of sensitivity, specificity, and reproducibility of an optimized method for detecting clonal rearrangements of immunoglobulin and T-cell receptor genes in formalin-fixed, paraffin-embedded sections. Diagn Mol Pathol. 1993 Dec;2(4):223–232. [PubMed] [Google Scholar]
  25. Tamura N., Holroyd K. J., Banks T., Kirby M., Okayama H., Crystal R. G. Diversity in junctional sequences associated with the common human V gamma 9 and V delta 2 gene segments in normal blood and lung compared with the limited diversity in a granulomatous disease. J Exp Med. 1990 Jul 1;172(1):169–181. doi: 10.1084/jem.172.1.169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Taylor J. J., Rowe D., Williamson I. K., Christmas S. E., Proctor S. J., Middleton P. G. Detection of T-cell receptor gamma chain V gene rearrangements using the polymerase chain reaction: application to the study of clonal disease cells in acute lymphoblastic leukemia. Blood. 1991 May 1;77(9):1989–1995. [PubMed] [Google Scholar]
  27. Trainor K. J., Brisco M. J., Wan J. H., Neoh S., Grist S., Morley A. A. Gene rearrangement in B- and T-lymphoproliferative disease detected by the polymerase chain reaction. Blood. 1991 Jul 1;78(1):192–196. [PubMed] [Google Scholar]
  28. Uppenkamp M., Andrade R., Sundeen J., Raffeld M., Coupland R., Cossman J. Diagnostic interpretation of T gamma gene rearrangement: effect of polyclonal T cells. Hematol Pathol. 1988;2(1):15–24. [PubMed] [Google Scholar]
  29. Uppenkamp M., Pittaluga S., Lipford E. H., Cossman J. Limited diversity and selection of rearranged gamma genes in polyclonal T cells. J Immunol. 1987 Mar 1;138(5):1618–1620. [PubMed] [Google Scholar]
  30. Volkenandt M., Soyer H. P., Cerroni L., Koch O. M., Atzpodien J., Kerl H. Molecular detection of clone-specific DNA in hypopigmented lesions of a patient with early evolving mycosis fungoides. Br J Dermatol. 1993 Apr;128(4):423–428. doi: 10.1111/j.1365-2133.1993.tb00203.x. [DOI] [PubMed] [Google Scholar]
  31. Volkenandt M., Soyer H. P., Kerl H., Bertino J. R. Development of a highly specific and sensitive molecular probe for detection of cutaneous lymphoma. J Invest Dermatol. 1991 Jul;97(1):137–140. doi: 10.1111/1523-1747.ep12479308. [DOI] [PubMed] [Google Scholar]
  32. Volkenandt M., Wienecke R., Koch O. M., Buer J., Probst M., Atzpodien J., Horikoshi T., Danenberg K., Danenberg P., Bertino J. R. Conformational polymorphisms of cRNA of T-cell-receptor genes as a clone-specific molecular marker for cutaneous lymphoma. J Invest Dermatol. 1993 Oct;101(4):514–516. doi: 10.1111/1523-1747.ep12365889. [DOI] [PubMed] [Google Scholar]
  33. d'Auriol L., Macintyre E., Galibert F., Sigaux F. In vitro amplification of T cell gamma gene rearrangements: a new tool for the assessment of minimal residual disease in acute lymphoblastic leukemias. Leukemia. 1989 Feb;3(2):155–158. [PubMed] [Google Scholar]

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