Mary Ellen Lane
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Mary Ellen Lane has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
Alexander P Runko
1 shared publicationAlexander P. Runko
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, 364 Plantation Street/LRB822, Worcester, MA 01605, USA
1 shared publicationAndrea Arguello
Department of Biochemistry and Cell Biology, Rice University, Houston, Texas
1 shared publication- Catherine W. McCollum
Center for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, TX 77204, USA
1 shared publication Charles G Sagerström
1 shared publicationCharles G. Sagerström
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, 364 Plantation Street/LRB822, Worcester, MA 01605, USA
1 shared publication
Latest Publications
- Open Access
- 29 October 2007
- Published by Wiley in Developmental Dynamics
- Vol. 236 (12) , 3427-3435
Zebrafish cdc25a is expressed during early development and limiting for post‐blastoderm cell cycle progression
Cdc25 phosphatases are required for eukaryotic cell cycle progression. To investigate mechanisms governing spatiotemporal dynamics of cell cycle progression during vertebrate development, we isolated two cdc25 genes from the zebrafish, Danio rerio, cdc25a, and cdc25d. We propose that Zebrafish cdc25a is the zebrafish orthologue of the tetrapod Cdc25A genes, while cdc25d is of indeterminate origin. We show that both genes have proliferation promoting activity, but that only cdc25d can complement a Schizosaccharomyces pombe loss of function cdc25 mutation. We present expression data demonstrating that cdc25d expression is very limited during early development, while cdc25a is widely expressed and consistent with the mitotic activity in previously identified mitotic domains of the post‐blastoderm zebrafish embryo. Finally, we show that cdc25a can accelerate the entry of post‐blastoderm cells into mitosis, suggesting that levels of cdc25a are rate limiting for cell cycle progression during gastrulation. Developmental Dynamics 236:3427–3435, 2007.
- 29 October 2007
- Published by Wiley in Developmental Dynamics
- Vol. 236 (12) , 3427-3435
Open AccessZebrafish cdc25a is expressed during early development and limiting for post‐blastoderm cell cycle progression
Cdc25 phosphatases are required for eukaryotic cell cycle progression. To investigate mechanisms governing spatiotemporal dynamics of cell cycle progression during vertebrate development, we isolated two cdc25 genes from the zebrafish, Danio rerio, cdc25a, and cdc25d. We propose that Zebrafish cdc25a is the zebrafish orthologue of the tetrapod Cdc25A genes, while cdc25d is of indeterminate origin. We show that both genes have proliferation promoting activity, but that only cdc25d can complement a Schizosaccharomyces pombe loss of function cdc25 mutation. We present expression data demonstrating that cdc25d expression is very limited during early development, while cdc25a is widely expressed and consistent with the mitotic activity in previously identified mitotic domains of the post‐blastoderm zebrafish embryo. Finally, we show that cdc25a can accelerate the entry of post‐blastoderm cells into mitosis, suggesting that levels of cdc25a are rate limiting for cell cycle progression during gastrulation. Developmental Dynamics 236:3427–3435, 2007.
- 15 September 2007
- Published by Elsevier in Developmental Biology
- Vol. 309 (2) , 373-385
A zebrafish LMO4 ortholog limits the size of the forebrain and eyes through negative regulation of six3b and rx3
- 15 September 2007
- Published by Elsevier in Developmental Biology
- Vol. 309 (2) , 373-385
A zebrafish LMO4 ortholog limits the size of the forebrain and eyes through negative regulation of six3b and rx3
- Retracted
- 31 December 2002
- Published by Elsevier in Gene Expression Patterns
- Vol. 2 (3-4) , 207-211
RETRACTED: Dynamic expression and regulation by Fgf8 and Pou2 of the zebrafish LIM-only gene, lmo4
- 31 December 2002
- Published by Elsevier in Gene Expression Patterns
- Vol. 2 (3-4) , 207-211
RetractedRETRACTED: Dynamic expression and regulation by Fgf8 and Pou2 of the zebrafish LIM-only gene, lmo4
- Retracted
- 1 December 2002
- Published by Elsevier in Mechanisms of Development
- Vol. 119, S185-S189
Dynamic expression and regulation by Fgf8 and Pou2 of the zebrafish LIM-only gene, lmo4
- 1 December 2002
- Published by Elsevier in Mechanisms of Development
- Vol. 119, S185-S189
RetractedDynamic expression and regulation by Fgf8 and Pou2 of the zebrafish LIM-only gene, lmo4