Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22

被引:41
|
作者
Curtiss, NP
Bonifas, JM
Lauchle, JO
Balkman, JD
Kratz, CP
Emerling, BM
Green, ED
Le Beau, MM
Shannon, KM
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] NHGRI, Genome Technol Branch, Bethesda, MD 20892 USA
[3] Univ Chicago, Hematol Oncol Sect, Dept Med, Chicago, IL 60637 USA
[4] Univ Chicago, Canc Res Ctr, Chicago, IL 60637 USA
关键词
chromosome; 7; acute myeloid leukemia; Myelodysplastic syndrome; monosomy; F-box proteins;
D O I
10.1016/j.ygeno.2005.01.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Monosomy 7 and deletions of 7q are recurring leukemia-associated cytogenetic abnormalities that correlate with adverse outcomes in children and adults. We describe a 2.52-Mb genomic DNA contig that spans a commonly deleted segment of chromosome band 7q22 identified in myeloid malignancies. This interval currently includes 14 genes, 19 predicted genes, and 5 predicted pseudogenes. We have extensively characterized the FBXL13, NAPE-PLD, and SVH genes as candidate myeloid tumor suppressors. FBXL13 encodes a novel F-box protein, SVHis a member of a gene family that contains Armadillo-like repeats, and NAPE-PLD encodes a phospholipase D-type phosphodiesterase. Analysis of a panel of leukemia specimens with monosomy 7 did not reveal mutations in these or in the candidate genes LRRC17, PRO1598,and SRPK2. This fully sequenced and annotated contig provides a resource for candidate myeloid tumor suppressor gene discovery. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:600 / 607
页数:8
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