## Abstract Because of its genetic, molecular, and behavioral tractability, __Drosophila__ has emerged as a powerful model system for studying molecular and cellular mechanisms underlying the development and function of nervous systems. The __Drosophila__ nervous system has fewer neurons and exhibi
New hemocyte-specific enhancer-reporter transgenes for the analysis of hematopoiesis in Drosophila
✍ Scribed by Tsuyoshi Tokusumi; Douglas A. Shoue; Yumiko Tokusumi; Jessica R. Stoller; Robert A. Schulz
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 364 KB
- Volume
- 47
- Category
- Article
- ISSN
- 1526-954X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Based on environmental challenges or altered genetic composition, Drosophila larvae can produce up to three types of blood cells that express genetic programs essential for their distinct functions. Using transcriptional enhancers for genes expressed exclusively in plasmatocytes, crystal cells, or lamellocytes, several new hemocyte‐specific enhancer‐reporter transgenes were generated to facilitate the analysis of Drosophila hematopoiesis. This approach took advantage of fluorescent variants of insulated P‐element reporter vectors for multilabeling cell analyses; two additional color variants were generated in these studies. These vectors were successfully used to produce transgenic fly lines that label specific hemocyte lineages with separate colors. Combining three transgene reporters allowed for the unambiguous identification of plasmatocytes, crystal cells, and lamellocytes within a complex hemocyte population. While this work focused on the hematopoietic process, these new vectors can be used to mark multiple cell types or trace complex cell lineages during any chosen aspect of Drosophila development. genesis 47:771–774, 2009. © 2009 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract **Designer label**: A newly developed polarity‐sensitive fluorescent probe (DBHA) was combined with a tyrosine‐specific labelling method that uses transition metal catalysis, and was successfully used in local structural analysis of the Tyr108 domain in Cu/Zn superoxide dismutase (SOD;