| Literature DB >> 19924812 |
Stephanie E Gline1, Dian-Han Kuo, Alberto Stolfi, David A Weisblat.
Abstract
Knowing the normal patterns of embryonic cell proliferation, migration, and differentiation is a cornerstone for understanding development. Yet for most species, the precision with which embryonic cell lineages can be determined is limited by technical considerations (the large numbers of cells, extended developmental times, opacity of the embryos), and these are exacerbated by the inherent variability of the lineages themselves. Here, we present an improved method of cell lineage tracing in the leech Helobdella, driving the expression of a nuclearly localized histone H2B:GFP (green fluorescent protein) fusion protein in selected lineages by microinjection of a plasmid vector. This construct generates a long lasting and minimally mosaic signal with single cell resolution, and does not disrupt the development of most lineages tested. We have validated this technique by elucidating details of cell lineages contributing to segmental and prostomial tissues that could not be observed with standard dextran lineage tracers. (c) 2009 Wiley-Liss, Inc.Entities:
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Year: 2009 PMID: 19924812 PMCID: PMC3086637 DOI: 10.1002/dvdy.22158
Source DB: PubMed Journal: Dev Dyn ISSN: 1058-8388 Impact factor: 3.780