» Articles » PMID: 15492775

Whole-genome Analysis of Temporal Gene Expression During Foregut Development

Overview
Journal PLoS Biol
Specialty Biology
Date 2004 Oct 20
PMID 15492775
Citations 52
Authors
Affiliations
Soon will be listed here.
Abstract

We have investigated the cis-regulatory network that mediates temporal gene expression during organogenesis. Previous studies demonstrated that the organ selector gene pha-4/FoxA is critical to establish the onset of transcription of Caenorhabditis elegans foregut (pharynx) genes. Here, we discover additional cis-regulatory elements that function in combination with PHA-4. We use a computational approach to identify candidate cis-regulatory sites for genes activated either early or late during pharyngeal development. Analysis of natural or synthetic promoters reveals that six of these sites function in vivo. The newly discovered temporal elements, together with predicted PHA-4 sites, account for the onset of expression of roughly half of the pharyngeal genes examined. Moreover, combinations of temporal elements and PHA-4 sites can be used in genome-wide searches to predict pharyngeal genes, with more than 85% accuracy for their onset of expression. These findings suggest a regulatory code for temporal gene expression during foregut development and provide a means to predict gene expression patterns based solely on genomic sequence.

Citing Articles

Unconventional Myosins from as a Probe to Study Human Orthologues.

Johnson C, Behbehani R, Buss F Biomolecules. 2022; 12(12).

PMID: 36551317 PMC: 9775386. DOI: 10.3390/biom12121889.


The emergent role of mitochondrial surveillance in cellular health.

Tjahjono E, Kirienko D, Kirienko N Aging Cell. 2022; 21(11):e13710.

PMID: 36088658 PMC: 9649602. DOI: 10.1111/acel.13710.


Feedforward regulatory logic controls the specification-to-differentiation transition and terminal cell fate during Caenorhabditis elegans endoderm development.

Ewe C, Sommermann E, Kenchel J, Flowers S, Maduro M, Joshi P Development. 2022; 149(12).

PMID: 35758255 PMC: 10656426. DOI: 10.1242/dev.200337.


Evolutionary Dynamics of the SKN-1 → MED → END-1,3 Regulatory Gene Cascade in Endoderm Specification.

Maduro M G3 (Bethesda). 2019; 10(1):333-356.

PMID: 31740453 PMC: 6945043. DOI: 10.1534/g3.119.400724.


Reduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development.

Zheleva A, Gomez-Orte E, Saenz-Narciso B, Ezcurra B, Kassahun H, de Toro M PLoS Genet. 2019; 15(9):e1008338.

PMID: 31525188 PMC: 6762213. DOI: 10.1371/journal.pgen.1008338.


References
1.
Thatcher J, Fernandez A, Haun C, Okkema P . The Caenorhabditis elegans peb-1 gene encodes a novel DNA-binding protein involved in morphogenesis of the pharynx, vulva, and hindgut. Dev Biol. 2001; 229(2):480-93. DOI: 10.1006/dbio.2000.9978. View

2.
Dufort D, Schwartz L, Harpal K, Rossant J . The transcription factor HNF3beta is required in visceral endoderm for normal primitive streak morphogenesis. Development. 1998; 125(16):3015-25. DOI: 10.1242/dev.125.16.3015. View

3.
Kemphues K, Priess J, Morton D, Cheng N . Identification of genes required for cytoplasmic localization in early C. elegans embryos. Cell. 1988; 52(3):311-20. DOI: 10.1016/s0092-8674(88)80024-2. View

4.
Jiang M, Ryu J, Kiraly M, Duke K, Reinke V, Kim S . Genome-wide analysis of developmental and sex-regulated gene expression profiles in Caenorhabditis elegans. Proc Natl Acad Sci U S A. 2001; 98(1):218-23. PMC: 14571. DOI: 10.1073/pnas.98.1.218. View

5.
KELLY W, Xu S, Montgomery M, Fire A . Distinct requirements for somatic and germline expression of a generally expressed Caernorhabditis elegans gene. Genetics. 1997; 146(1):227-38. PMC: 1207937. DOI: 10.1093/genetics/146.1.227. View