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Molecular identification of ADP-ribosylation factor mRNAs and their expression in mammalian cells
M Tsuchiya1, S R Price, S C Tsai
1Laboratory of Cellular Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.
Abstract:
ADP-ribosylation factors (ARFs) are approximately 20-kDa guanine nucleotide-binding proteins that serve as GTP-dependent allosteric activators of cholera toxin ADP-ribosyltransferase activity. Four species of mammalian ARF, termed ARF 1-4, have been identified by cloning. Hybridization of a bovine ARF 2 cDNA under low stringency with mammalian poly(A)+ RNA resulted in multiple bands that were subsequently assigned to the known ARF genes using ARF-specific oligonucleotide probes. The relative signal intensities of some bands (e.g. the 3.8- and 1.3-kilobase (kb) mRNAs) that hybridized with the cDNA were not, however, consistent with the intensities observed with the individual ARF-specific oligonucleotide probes. These inconsistencies suggested that other ARF-like mRNAs were comigrating with known ARF mRNAs. To explore this possibility, a cyclic AMP-differentiated HL-60 Lambda ZAP library was screened using the bovine ARF 2 cDNA. Clones corresponding to known ARF genes (1, 3, and 4) were identified by hybridization of positive clones with oligonucleotide probes specific for each ARF species; ARF 2 cDNA-positive, oligonucleotide-negative clones were sequenced. Two new ARF-like genes, ARF 5 and 6, encoding proteins of 180 and 175 amino acids, respectively, were identified. Both proteins contain consensus sequences believed to be involved in guanine nucleotide binding and GTP hydrolysis. ARF 5 was most similar in deduced amino acid sequence to ARF 4, which also has 180 amino acids. ARF 6, whose deduced amino acid sequence is identical with that of a putative chicken pseudogene (CPS1) except for a serine/threonine substitution, was different from other ARF species in size and deduced amino acid sequence. With mammalian poly(A)+ RNA from a variety of tissues and cultured cells, ARF 5 preferentially hybridized with a 1.3-kb mRNA, whereas ARF 6 hybridized with 1.8- and 4.2-kb mRNAs. The fact that the sizes of these mRNAs are similar to those of other ARFs (ARF 1, 1.9 kb; ARF 2, 2.6 kb; ARF 3, approximately 3.8 and 1.3 kb; ARF 4, 1.8 kb) explain the previously observed inconsistencies between the cDNA and ARF-specific oligonucleotide hybridization patterns. All six ARF cDNAs are more similar to each other than to other approximately 20-kDa guanine nucleotide-binding proteins.
Insights
Researchers discovered two novel ADP-ribosylation factors (ARFs), ARF 5 and ARF 6, expanding the known ARF gene family. These findings help explain previous inconsistencies in ARF gene expression analysis.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- ADP-ribosylation factors (ARFs) are crucial 20-kDa guanine nucleotide-binding proteins.
- ARFs function as GTP-dependent activators of cholera toxin ADP-ribosyltransferase.
- Four mammalian ARF species (ARF 1-4) were previously identified through cloning.
Purpose of the Study:
- To investigate inconsistencies in ARF gene expression analysis.
- To identify novel ARF-like genes and their corresponding mRNAs.
- To expand the understanding of the ARF gene family.
Main Methods:
- Screening of a HL-60 Lambda ZAP library using bovine ARF 2 cDNA.
- Hybridization with ARF-specific oligonucleotide probes.
- Sequencing of ARF 2 cDNA-positive, oligonucleotide-negative clones.
- Analysis of mRNA expression patterns using mammalian poly(A)+ RNA.
Main Results:
- Identification of two new ARF-like genes: ARF 5 and ARF 6.
- ARF 5 and ARF 6 encode proteins with conserved guanine nucleotide-binding and GTP hydrolysis motifs.
- ARF 5 exhibits sequence similarity to ARF 4; ARF 6 is distinct and similar to a chicken pseudogene.
- ARF 5 preferentially hybridizes to a 1.3-kb mRNA, while ARF 6 hybridizes to 1.8- and 4.2-kb mRNAs.
Conclusions:
- The discovery of ARF 5 and ARF 6 resolves previous hybridization inconsistencies.
- The distinct mRNA sizes of ARF 5 and ARF 6 explain observed discrepancies in gene expression analysis.
- All six identified ARF cDNAs share significant similarity, suggesting a conserved functional role within the ARF family.