Structure of the Dictyostelium discoideum prestalk D11 gene and protein.
Open Access
- 1 June 1985
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 5 (6) , 1473-1479
- https://doi.org/10.1128/mcb.5.6.1473
Abstract
The gene encoding the prestalk D11 mRNA of Dictyostelium discoideum has been isolated and characterized. Transcriptional mapping and sequence data indicated that the D11 message is unspliced and contains an 846-base open reading frame. The 273 base pairs upstream from the translation initiator codon are 88% A + T, typical of Dictyostelium upstream sequences, and contain no recognizable upstream activator sequence. The deduced D11 protein is exceptionally rich in cysteine residues and consists of a 25-amino acid hydrophobic leader sequence (L) followed by a series of repeats with the structure LA1B1A2B2C1B3C2B4C3B5C4B6, where A, B, and C, are, respectively, amino acid sequences of 39, 18, and 15 residues. The deduced D11 protein shares certain similarities with the Dictyostelium cyclic AMP phosphodiesterase inhibitor protein.This publication has 18 references indexed in Scilit:
- [57] Sequencing end-labeled DNA with base-specific chemical cleavagesPublished by Elsevier ,2004
- Mechanism of sequential induction of cell-type specific mRNAs in Dictyostelium differentiationNature, 1984
- Three different fibronectin mRNAs arise by alternative splicing within the coding regionCell, 1983
- Structure of the plasmodium knowlesi gene coding for the circumsporozoite proteinCell, 1983
- Regulation of dictyostelium discoideum mRNAs specific for prespore or prestalk cellsCell, 1983
- An expandable gene that encodes a Drosophila glue protein is not expressed in variants lacking remote upstream sequencesCell, 1982
- Synthesis and stability of developmentally regulated dictyostelium mRNAs are affected by cell-cell contact and cAMPCell, 1981
- Construction of coliphage lambda Charon vectors with BamHI cloning sitesGene, 1980
- Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybridsCell, 1977
- Screening λgt Recombinant Clones by Hybridization to Single Plaques in SituScience, 1977