## Abstract Myeloid sarcoma (MS) is a tumor mass of myeloblasts or immature myeloid cells occurring in an extramedullary site. In this study, seven cases of MS [stomach (1), testis (1), skin (2), and lymph node (3)] and 3 synchronous and 1 followβup bone marrow (BM) samples were studied for genomic
Construction and application of a zebrafish array comparative genomic hybridization platform
β Scribed by Jennifer L. Freeman; Craig Ceol; Hui Feng; David M. Langenau; Cassandra Belair; Howard M. Stern; Anhua Song; Barry H. Paw; A. Thomas Look; Yi Zhou; Leonard I. Zon; Charles Lee
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 243 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1045-2257
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β¦ Synopsis
Abstract
The zebrafish is emerging as a prominent model system for studying the genetics of human development and disease. Genetic alterations that underlie each mutant model can exist in the form of single base changes, balanced chromosomal rearrangements, or genetic imbalances. To detect genetic imbalances in an unbiased genomeβwide fashion, array comparative genomic hybridization (CGH) can be used. We have developed a 5βMb resolution array CGH platform specifically for the zebrafish. This platform contains 286 bacterial artificial chromosome (BAC) clones, enriched for orthologous sequences of human oncogenes and tumor suppressor genes. Each BAC clone has been endβsequenced and cytogenetically assigned to a specific location within the zebrafish genome, allowing for ease of integration of array CGH data with the current version of the genome assembly. This platform has been applied to three zebrafish cancer models. Significant genomic imbalances were detected in each model, identifying different regions that may potentially play a role in tumorigenesis. Hence, this platform should be a useful resource for genetic dissection of additional zebrafish developmental and disease models as well as a benchmark for future array CGH platform development. Β© 2008 WileyβLiss, Inc.
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