author_facet Cario, Gunnar
Stadt, Udo zur
Reiter, Alfred
Welte, Karl
Sykora, Karl‐Walter
Cario, Gunnar
Stadt, Udo zur
Reiter, Alfred
Welte, Karl
Sykora, Karl‐Walter
author Cario, Gunnar
Stadt, Udo zur
Reiter, Alfred
Welte, Karl
Sykora, Karl‐Walter
spellingShingle Cario, Gunnar
Stadt, Udo zur
Reiter, Alfred
Welte, Karl
Sykora, Karl‐Walter
British Journal of Haematology
Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
Hematology
author_sort cario, gunnar
spelling Cario, Gunnar Stadt, Udo zur Reiter, Alfred Welte, Karl Sykora, Karl‐Walter 0007-1048 1365-2141 Wiley Hematology http://dx.doi.org/10.1046/j.1365-2141.2000.02241.x <jats:p>Burkitt's lymphoma/Burkitt cell leukaemia (BL) is characterized by one of the reciprocal translocations involving the MYC oncogene on chromosome 8 and one of the immunoglobulin (Ig) loci on chromosomes 14, 2 or 22. In the few cell lines with the variant translocations t(2;8) and t(8;22) reported to date, the breakpoints on chromosome 8 were located downstream of MYC at a distance of up to 300 kb and more. Here, we describe three new cases with variant translocations. Fresh tumour material from paediatric patients, negative for the common translocation t(8;14), was analysed using a long‐distance (LD) polymerase chain reaction (PCR) approach. On chromosome 8, primers were derived from several different regions 3′ of MYC, and on chromosomes 2 and 22 from the constant regions of the Ig kappa (Igκ) and lambda (Igλ) genes. One translocation t(2;8) and two t(8;22) were detected. In the t(2;8) translocation, the chromosome 8 breakpoint was located 2 kb 3′ of the MYC exon 3 and the chromosome 2 breakpoint within an unrearranged Igκ locus. The breakpoints of the two translocations t(8;22) were detected 16 kb for one and 58 kb for the other downstream of MYC. Sequencing the t(8;22) translocation in one of the cases showed hypermutation of the translocated variable Vλ4b gene. The presence of hypermutated variable regions in the t(8;22) case suggests germinal centre B cells as the origin of this translocation. The t(2;8) translocation is the first description of a translocation t(2;8) involving an unrearranged Igκ gene. A mechanism different from V–J recombination and somatic hypermutation has to be proposed for this translocation.</jats:p> Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases British Journal of Haematology
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title Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_unstemmed Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_full Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_fullStr Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_full_unstemmed Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_short Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_sort variant translocations in sporadic burkitt's lymphoma detected in fresh tumour material: analysis of three cases
topic Hematology
url http://dx.doi.org/10.1046/j.1365-2141.2000.02241.x
publishDate 2000
physical 537-546
description <jats:p>Burkitt's lymphoma/Burkitt cell leukaemia (BL) is characterized by one of the reciprocal translocations involving the MYC oncogene on chromosome 8 and one of the immunoglobulin (Ig) loci on chromosomes 14, 2 or 22. In the few cell lines with the variant translocations t(2;8) and t(8;22) reported to date, the breakpoints on chromosome 8 were located downstream of MYC at a distance of up to 300 kb and more. Here, we describe three new cases with variant translocations. Fresh tumour material from paediatric patients, negative for the common translocation t(8;14), was analysed using a long‐distance (LD) polymerase chain reaction (PCR) approach. On chromosome 8, primers were derived from several different regions 3′ of MYC, and on chromosomes 2 and 22 from the constant regions of the Ig kappa (Igκ) and lambda (Igλ) genes. One translocation t(2;8) and two t(8;22) were detected. In the t(2;8) translocation, the chromosome 8 breakpoint was located 2 kb 3′ of the MYC exon 3 and the chromosome 2 breakpoint within an unrearranged Igκ locus. The breakpoints of the two translocations t(8;22) were detected 16 kb for one and 58 kb for the other downstream of MYC. Sequencing the t(8;22) translocation in one of the cases showed hypermutation of the translocated variable Vλ4b gene. The presence of hypermutated variable regions in the t(8;22) case suggests germinal centre B cells as the origin of this translocation. The t(2;8) translocation is the first description of a translocation t(2;8) involving an unrearranged Igκ gene. A mechanism different from V–J recombination and somatic hypermutation has to be proposed for this translocation.</jats:p>
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author Cario, Gunnar, Stadt, Udo zur, Reiter, Alfred, Welte, Karl, Sykora, Karl‐Walter
author_facet Cario, Gunnar, Stadt, Udo zur, Reiter, Alfred, Welte, Karl, Sykora, Karl‐Walter, Cario, Gunnar, Stadt, Udo zur, Reiter, Alfred, Welte, Karl, Sykora, Karl‐Walter
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description <jats:p>Burkitt's lymphoma/Burkitt cell leukaemia (BL) is characterized by one of the reciprocal translocations involving the MYC oncogene on chromosome 8 and one of the immunoglobulin (Ig) loci on chromosomes 14, 2 or 22. In the few cell lines with the variant translocations t(2;8) and t(8;22) reported to date, the breakpoints on chromosome 8 were located downstream of MYC at a distance of up to 300 kb and more. Here, we describe three new cases with variant translocations. Fresh tumour material from paediatric patients, negative for the common translocation t(8;14), was analysed using a long‐distance (LD) polymerase chain reaction (PCR) approach. On chromosome 8, primers were derived from several different regions 3′ of MYC, and on chromosomes 2 and 22 from the constant regions of the Ig kappa (Igκ) and lambda (Igλ) genes. One translocation t(2;8) and two t(8;22) were detected. In the t(2;8) translocation, the chromosome 8 breakpoint was located 2 kb 3′ of the MYC exon 3 and the chromosome 2 breakpoint within an unrearranged Igκ locus. The breakpoints of the two translocations t(8;22) were detected 16 kb for one and 58 kb for the other downstream of MYC. Sequencing the t(8;22) translocation in one of the cases showed hypermutation of the translocated variable Vλ4b gene. The presence of hypermutated variable regions in the t(8;22) case suggests germinal centre B cells as the origin of this translocation. The t(2;8) translocation is the first description of a translocation t(2;8) involving an unrearranged Igκ gene. A mechanism different from V–J recombination and somatic hypermutation has to be proposed for this translocation.</jats:p>
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spelling Cario, Gunnar Stadt, Udo zur Reiter, Alfred Welte, Karl Sykora, Karl‐Walter 0007-1048 1365-2141 Wiley Hematology http://dx.doi.org/10.1046/j.1365-2141.2000.02241.x <jats:p>Burkitt's lymphoma/Burkitt cell leukaemia (BL) is characterized by one of the reciprocal translocations involving the MYC oncogene on chromosome 8 and one of the immunoglobulin (Ig) loci on chromosomes 14, 2 or 22. In the few cell lines with the variant translocations t(2;8) and t(8;22) reported to date, the breakpoints on chromosome 8 were located downstream of MYC at a distance of up to 300 kb and more. Here, we describe three new cases with variant translocations. Fresh tumour material from paediatric patients, negative for the common translocation t(8;14), was analysed using a long‐distance (LD) polymerase chain reaction (PCR) approach. On chromosome 8, primers were derived from several different regions 3′ of MYC, and on chromosomes 2 and 22 from the constant regions of the Ig kappa (Igκ) and lambda (Igλ) genes. One translocation t(2;8) and two t(8;22) were detected. In the t(2;8) translocation, the chromosome 8 breakpoint was located 2 kb 3′ of the MYC exon 3 and the chromosome 2 breakpoint within an unrearranged Igκ locus. The breakpoints of the two translocations t(8;22) were detected 16 kb for one and 58 kb for the other downstream of MYC. Sequencing the t(8;22) translocation in one of the cases showed hypermutation of the translocated variable Vλ4b gene. The presence of hypermutated variable regions in the t(8;22) case suggests germinal centre B cells as the origin of this translocation. The t(2;8) translocation is the first description of a translocation t(2;8) involving an unrearranged Igκ gene. A mechanism different from V–J recombination and somatic hypermutation has to be proposed for this translocation.</jats:p> Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases British Journal of Haematology
spellingShingle Cario, Gunnar, Stadt, Udo zur, Reiter, Alfred, Welte, Karl, Sykora, Karl‐Walter, British Journal of Haematology, Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases, Hematology
title Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_full Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_fullStr Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_full_unstemmed Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_short Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_sort variant translocations in sporadic burkitt's lymphoma detected in fresh tumour material: analysis of three cases
title_unstemmed Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases
topic Hematology
url http://dx.doi.org/10.1046/j.1365-2141.2000.02241.x