In our review of the use of C. elegans as a biosensor (Lindblom and Dodd, 2006), we regrettably misrepresented the work of Dr. Cristina Lagido and colleagues when we inadvertently compared their use of bacterial and eukaryotic luciferase enzymes in C. elegans. We stated on page 726 that One study ut
Endomesoderm specification in Caenorhabditis elegans and other nematodes
β Scribed by Morris F. Maduro
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 419 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0265-9247
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The endomesoderm gene regulatory network (GRN) of C. elegans is a rich resource for studying the properties of cellβfateβspecification pathways. This GRN contains both cellβautonomous and cell nonβautonomous mechanisms, includes network motifs found in other GRNs, and ties maternal factors to terminal differentiation genes through a regulatory cascade. In most cases, upstream regulators and their direct downstream targets are known. With the availability of resources to study close and distant relatives of C. elegans, the molecular evolution of this network can now be examined. Within Caenorhabditis, components of the endomesoderm GRN are well conserved. A cursory examination of the preliminary genome sequences of two parasitic nematodes, Haemonchus contortus and Brugia malayi, suggests that evolution in this GRN is occurring most rapidly for the zygotic genes that specify blastomere identity. BioEssays 28: 1010β1022, 2006. Β© 2006 Wiley Periodicals, Inc.
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