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The JAK2 46/1 haplotype predisposes to MPL mutated myeloproliferative neoplasms

The JAK2 46/1 haplotype predisposes to MPL mutated myeloproliferative neoplasms
The JAK2 46/1 haplotype predisposes to MPL mutated myeloproliferative neoplasms
The 46/1 JAK2 haplotype predisposes to V617F-positive myeloproliferative neoplasms but the underlying mechanism is obscure. We analyzed essential thrombocythemia patients entered into the PT-1 studies and, as expected, found that 46/1 was overrepresented in V617F-positive cases (n=404) versus controls (n=1492; P=3.9x10(-11)). 46/1 was also overrepresented in cases without V617F (n=347, P=0.009), with an excess seen for both MPL exon 10 mutated and V617F, MPL exon 10 non-mutated cases. Analysis of further MPL-positive, V617F-negative cases confirmed an excess of 46/1 (n=176, P=0.002) but no association between MPL mutations and MPL haplotype was seen. An excess of 46/1 was also seen in JAK2 exon 12 mutated cases (n=69, P=0.002) and these mutations preferentially arose on the 46/1 chromosome (P=0.029). No association between 46/1 and clinical or laboratory features was seen in the PT-1 cohort either with or without V617F. The excess of 46/1 in JAK2 exon 12 mutated cases is compatible with both the 'hypermutability' and 'fertile ground' hypotheses, but the excess in MPL mutated cases argues against the former. No difference in sequence, splicing or expression of JAK2 was found on 46/1 compared to other haplotypes suggesting that any functional difference of JAK2 on 46/1, if it exists, must be relatively subtle.
0006-4971
4517-4523
Jones, Amy V.
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Campbell, Peter J.
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Beer, Philip A.
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Schnittger, Sussane
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Vannucchi, Alessandro M.
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Zoi, Katerina
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Percy, Melanie J.
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McMullin, Mary Frances
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Scott, Linda M.
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Tapper, William
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Silver, Richard T.
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Oscier, D.
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Harrison, Claire N.
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Grallert, Harald
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Kisialiou, Aliaksei
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Strike, Paul
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Chase, Andrew J.
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Green, Anthony R.
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Cross, Nicholas C.P.
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Jones, Amy V.
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Campbell, Peter J.
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Beer, Philip A.
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Schnittger, Sussane
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Vannucchi, Alessandro M.
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Zoi, Katerina
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Percy, Melanie J.
3931fb83-92f0-4aca-a135-7d887836c750
McMullin, Mary Frances
feeaf619-229b-4827-ae20-29b9b2b03bf9
Scott, Linda M.
e171f5f7-72d4-4ba6-9a95-ce63403f0158
Tapper, William
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Silver, Richard T.
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Oscier, D.
c2620a1d-25bb-48f7-9651-f5d023636381
Harrison, Claire N.
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Grallert, Harald
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Kisialiou, Aliaksei
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Strike, Paul
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Chase, Andrew J.
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Green, Anthony R.
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Cross, Nicholas C.P.
f87650da-b908-4a34-b31b-d62c5f186fe4

Jones, Amy V., Campbell, Peter J., Beer, Philip A., Schnittger, Sussane, Vannucchi, Alessandro M., Zoi, Katerina, Percy, Melanie J., McMullin, Mary Frances, Scott, Linda M., Tapper, William, Silver, Richard T., Oscier, D., Harrison, Claire N., Grallert, Harald, Kisialiou, Aliaksei, Strike, Paul, Chase, Andrew J., Green, Anthony R. and Cross, Nicholas C.P. (2010) The JAK2 46/1 haplotype predisposes to MPL mutated myeloproliferative neoplasms. Blood, 115 (22), 4517-4523. (doi:10.1182/blood-2009-08-236448).

Record type: Article

Abstract

The 46/1 JAK2 haplotype predisposes to V617F-positive myeloproliferative neoplasms but the underlying mechanism is obscure. We analyzed essential thrombocythemia patients entered into the PT-1 studies and, as expected, found that 46/1 was overrepresented in V617F-positive cases (n=404) versus controls (n=1492; P=3.9x10(-11)). 46/1 was also overrepresented in cases without V617F (n=347, P=0.009), with an excess seen for both MPL exon 10 mutated and V617F, MPL exon 10 non-mutated cases. Analysis of further MPL-positive, V617F-negative cases confirmed an excess of 46/1 (n=176, P=0.002) but no association between MPL mutations and MPL haplotype was seen. An excess of 46/1 was also seen in JAK2 exon 12 mutated cases (n=69, P=0.002) and these mutations preferentially arose on the 46/1 chromosome (P=0.029). No association between 46/1 and clinical or laboratory features was seen in the PT-1 cohort either with or without V617F. The excess of 46/1 in JAK2 exon 12 mutated cases is compatible with both the 'hypermutability' and 'fertile ground' hypotheses, but the excess in MPL mutated cases argues against the former. No difference in sequence, splicing or expression of JAK2 was found on 46/1 compared to other haplotypes suggesting that any functional difference of JAK2 on 46/1, if it exists, must be relatively subtle.

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Accepted/In Press date: 19 March 2010
Published date: 3 June 2010

Identifiers

Local EPrints ID: 143547
URI: http://eprints.soton.ac.uk/id/eprint/143547
ISSN: 0006-4971
PURE UUID: 135b7204-e2ac-4677-9a7c-83f4bfb703b8
ORCID for William Tapper: ORCID iD orcid.org/0000-0002-5896-1889
ORCID for Andrew J. Chase: ORCID iD orcid.org/0000-0001-6617-9953
ORCID for Nicholas C.P. Cross: ORCID iD orcid.org/0000-0001-5481-2555

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Date deposited: 12 Apr 2010 11:52
Last modified: 14 Mar 2024 02:46

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Contributors

Author: Amy V. Jones
Author: Peter J. Campbell
Author: Philip A. Beer
Author: Sussane Schnittger
Author: Alessandro M. Vannucchi
Author: Katerina Zoi
Author: Melanie J. Percy
Author: Mary Frances McMullin
Author: Linda M. Scott
Author: William Tapper ORCID iD
Author: Richard T. Silver
Author: D. Oscier
Author: Claire N. Harrison
Author: Harald Grallert
Author: Aliaksei Kisialiou
Author: Paul Strike
Author: Andrew J. Chase ORCID iD
Author: Anthony R. Green

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