Literature DB >> 8436297

CAR2, a prestalk cAMP receptor required for normal tip formation and late development of Dictyostelium discoideum.

C L Saxe1, G T Ginsburg, J M Louis, R Johnson, P N Devreotes, A R Kimmel.   

Abstract

Extracellular cAMP serves as a primary signaling molecule to regulate the development of Dictyostelium discoideum. It is required for chemotaxis, aggregation, cytodifferentiation, and morphogenetic movement. The receptors for cAMP are members of the family of cell-surface receptors that are linked to G proteins and characterized by seven putative transmembrane domains. Previously, we have isolated the gene for the cAMP receptor subtype 1 (CAR1) from Dictyostelium and suggested that several genes related to CAR1 were present in the genome. Here, we describe a family of cAMP receptor genes of Dictyostelium and the isolation and function of the gene for the cAMP receptor subtype 2, CAR2. CAR2 is structurally similar to CAR1. Overall, their transmembrane and loop domains are approximately 75% identical in amino acid sequence; however, their carboxyl termini are quite dissimilar; CAR2 possesses homopolymeric runs of histidines and asparagines that are absent from the corresponding region in CAR1. Although CAR1 is maximally expressed during the early stages of development, CAR2 is expressed only after cells have aggregated and, then, preferentially in prestalk cells. Transgenic Dictyostelium that have had their wild-type CAR2 gene replaced by a defective copy using homologous recombination proceed through early development but are detained at the tight mound stage. CAR2 may be required for cAMP-directed sorting of prestalk cells during pattern formation within the aggregation mound. Furthermore, although prestalk genes are expressed normally in aggregates that lack CAR2, they exhibit an enhanced expression of prespore-specific mRNA. Previously, we had shown that there was a requirement for CAR1 during early development. The present results demonstrate that the multiple responses of Dictyostelium to cAMP are regulated by distinct cAMP receptors that are encoded by unique genes.

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Year:  1993        PMID: 8436297     DOI: 10.1101/gad.7.2.262

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  38 in total

Review 1.  Learning from the slime mold: Dictyostelium and human disease.

Authors:  C L Saxe
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

Review 2.  cAMP signaling in Dictyostelium. Complexity of cAMP synthesis, degradation and detection.

Authors:  Shweta Saran; Marcel E Meima; Elisa Alvarez-Curto; Karin E Weening; Daniel E Rozen; Pauline Schaap
Journal:  J Muscle Res Cell Motil       Date:  2002       Impact factor: 2.698

3.  A ubiquitin-conjugating enzyme is essential for developmental transitions in Dictyostelium.

Authors:  A Clark; A Nomura; S Mohanty; R A Firtel
Journal:  Mol Biol Cell       Date:  1997-10       Impact factor: 4.138

4.  Identification and characterization of a novel alpha-kinase with a von Willebrand factor A-like motif localized to the contractile vacuole and Golgi complex in Dictyostelium discoideum.

Authors:  Venkaiah Betapudi; Cynthia Mason; Lucila Licate; Thomas T Egelhoff
Journal:  Mol Biol Cell       Date:  2005-02-23       Impact factor: 4.138

Review 5.  Genetic networks that regulate development in Dictyostelium cells.

Authors:  W F Loomis
Journal:  Microbiol Rev       Date:  1996-03

Review 6.  Role of PKA in the timing of developmental events in Dictyostelium cells.

Authors:  W F Loomis
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

7.  Acanthamoeba and Dictyostelium Use Different Foraging Strategies.

Authors:  Nick A Kuburich; Nirakar Adhikari; Jeffrey A Hadwiger
Journal:  Protist       Date:  2016-09-06

8.  Spatial and temporal expression of the Dictyostelium discoideum G alpha protein subunit G alpha 2: expression of a dominant negative protein inhibits proper prestalk to stalk differentiation.

Authors:  F Carrel; S Dharmawardhane; A M Clark; J A Powell-Coffman; R A Firtel
Journal:  Mol Biol Cell       Date:  1994-01       Impact factor: 4.138

9.  Possible cooperation of differential adhesion and chemotaxis in mound formation of Dictyostelium.

Authors:  Y Jiang; H Levine; J Glazier
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

10.  The surface cyclic AMP receptors, cAR1, cAR2, and cAR3, promote Ca2+ influx in Dictyostelium discoideum by a G alpha 2-independent mechanism.

Authors:  J L Milne; P N Devreotes
Journal:  Mol Biol Cell       Date:  1993-03       Impact factor: 4.138

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