Molecular characterization of NAD:arginine ADP-ribosyltransferase from rabbit skeletal muscle.

dc.creatorZolkiewska, A
dc.creatorNightingale, M S
dc.creatorMoss, J
dc.date1992-12-01
dc.date.accessioned2026-08-03T01:49:39Z
dc.descriptionMono-ADP-ribosylation is a reversible modification of proteins, with NAD:arginine ADP-ribosyltransferases (EC 2.4.2.31) and ADP-ribosylarginine hydrolases (EC 3.2.2.19) catalyzing the opposing reactions in an ADP-ribosylation cycle. A membrane-associated arginine-specific (mono)-ADP-ribosyltransferase was purified 215,000-fold from rabbit skeletal muscle. On the basis of the amino acid sequences of HPLC-purified tryptic peptides, degenerate oligonucleotide primers were synthesized and used in a polymerase chain reaction (PCR)-based procedure to generate cDNA. A specific probe, based on PCR-generated sequence, was used to screen a rabbit skeletal muscle cDNA library. A composite cDNA sequence, obtained from library screening and rapid amplification of the 5' end of the cDNA, contained a 981-base-pair open reading frame, encoding a 36,134-Da protein. The deduced amino acid sequence contained the sequences of the tryptic peptides, hydrophobic amino and carboxyl termini, and two potential sites for N-linked glycosylation. Escherichia coli cells transformed with an expression vector containing transferase-specific sequence expressed ADP-ribosyltransferase activity. A transferase-specific oligonucleotide probe recognized a 4-kilobase mRNA expressed primarily in rabbit skeletal and cardiac muscle. There was no extended similarity in deduced amino acid sequences of the muscle transferase and several bacterial ADP-ribosylating toxins. The hydrophobic amino and carboxyl termini may represent a signal peptide and a site for a glycosyl-phosphatidylinositol anchor, respectively. IMAGES:
dc.identifierhttps://pmc.ncbi.nlm.nih.gov/articles/PMC50548/
dc.identifierhttps://pubmed.ncbi.nlm.nih.gov/1454819/
dc.identifierhttps://doi.org/10.1073/pnas.89.23.11352
dc.identifier.urihttps://repo.dare.co.zw/handle/123456789/160144
dc.languageen
dc.publisherNational Academy of Sciences
dc.sourceProc Natl Acad Sci U S A
dc.subjectResearch Article
dc.titleMolecular characterization of NAD:arginine ADP-ribosyltransferase from rabbit skeletal muscle.
dc.typeText

Files