Taxonomic distribution of proteins containing Dabb domains

The tree below includes only several representative species and genera. The complete taxonomic breakdown of all proteins containing Dabb domains can be accessed here. Click the counts or percentage values to display the corresponding proteins.

Transcript identification and profiling during salt stress and recovery ofPopulus euphratica.

Gu R, Fonseca S, Puskas LG, Hackler L Jr, Zvara A, Dudits D, Pais MS
Tree Physiol. 2004; 24: 265-76

Populus euphratica Oli. is a salt-tolerant species that can cope with upto 450 mM NaCl under hydroponic conditions and can tolerate highaccumulations of Na+ and Cl- in roots and leaves when grown in 300 mMNaCl. Transcript responses to salt stress and recovery were monitored bymicroarray hybridization of 315 cDNAs preselected by suppressionsubtractive hybridization. Transcripts of a heat-shock protein and ahydroxyproline-rich glycoprotein accumulated 1.5 and 3 h, respectively,after adding 300 mM NaCl to the culture medium. Transcripts significantlyup-regulated by salt stress included ionic and osmotic homeostasiselements such as magnesium transporter-like protein, syntaxin-likeprotein, seed imbibition protein and plasma membrane intrinsic protein;metabolism regulators like cytochrome P450, zinc finger protein, cleavagefactor and aminotransferase; and the photosynthesis-activating enzymeRubisco activase and photorespiration-related glycolate oxidase. Severalphotosynthesis-related transcripts were down-regulated in response to 72 hof salt stress but were up-regulated after long-term recovery (48 h).Sucrose synthase, ABC transporter, calmodulin, Pop3 peptide and aquaporinappeared to be actively involved in the process of plant recovery fromsalt stress. Several transcripts encoding proteins of unknown functionwere regulated by salt stress. Selected transcripts exhibiting alteredtranscript profiles in response to salt stress were also analyzed byreal-time quantitative PCR. Transcript analysis during salt stress andrecovery of this woody species revealed several genes and correspondingproteins deserving special attention in future studies of salt tolerancein woody species.

Structure of the hypothetical protein At3g17210 from Arabidopsis thaliana.

Lytle BL, Peterson FC, Kjer KL, Frederick RO, Zhao Q, Thao S, Bingman C, Johnson KA, Phillips GN Jr, Volkman BF
J Biomol NMR. 2004; 28: 397-400

Structure of ribulose 1,5-bisphosphate carboxylase/oxygenase gene clusterfrom a thermophilic hydrogen-oxidizing bacterium, Hydrogenophilusthermoluteolus, and phylogeny of the fructose 1,6-bisphosphate aldolaseencoded by cbbA in the cluster.

Hayashi NR, Terazono K, Kodama T, Igarashi Y
Biosci Biotechnol Biochem. 2000; 64: 61-71

Four genes, cbbO, cbbY, cbbA, and the pyruvate kinase gene (pyk), werefound downstream of ribulose 1,5-bisphosphate carboxylase/oxygenase(RubisCO) genes, cbbLS, from a thermophilic hydrogen-oxidizing bacterium,Hydrogenophilus thermoluteolus (formerly Pseudomonashydrogenothermophila). cbbO was similar to norD in the denitrificationgene cluster, and cbbY was similar to cbbY from other autotrophicbacteria. cbbA encoded fructose 1,6-bisphosphate aldolase (FBP aldolase);however, CbbA was little similar to other CbbA proteins. When CbbA wasoverexpressed in Escherichia coli, overproduction of CbbA was detected bySDS-PAGE. However, the cell extract had slightly higher activity than acell extract of E. coli without cbbA. Phylogenetic analysis showed classII FBP aldolase divided into classes IIA and IIB, and that CbbA from H.thermoluteolus was in class IIA. Activities of RubisCO and FBP aldolasewere examined under autotrophic, mixotrophic, and heterotrophicconditions. The activities of the two enzymes were regulatedindependently.