Clones encoding mammalian ADP-ribosylarginine hydrolases
AssigneeThe United States of America as represented by the Department of Health and Human Services
InventorsJoel Moss, Sally J. Stanley, Maria S. Nightingale, Lucia Monaco, James J. Murtagh, Jr., Tatsuyuki Takada
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Abstract
The present invention relates to the production of mammalian ADP-ribosylarginine hydrolases. These enzymes can be manufactured using recombinant DNA technology and are useful in regulation of proteins involved in key metabolic pathways.
Claims14
An isolated nucleic acid which consists of a sequence selected from the group consisting of Seq. I.D. No. 1, Seq. I.D. No. 9 and Seq. I.D. No. 11.
An isolated nucleic acid consisting of a sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:9 and SEQ ID NO:11, operably linked to a promoter.
A method of producing a mammalian ADP-ribosylarginine hydrolase by introducing into a suitable host cell an expression cassette having a promoter sequence operably linked to a DNA sequence consisting of sequences selected from the group consisting of Seq. I.D. No. 1 and Seq. I.D. No. 9 or to a human sequence encoding only a hydrolase wherein approximately 90% of the sequence is Seq. I.D. No. 11, and expressing said DNA sequence to produce said mammalian ADP-ribosylarginine hydrolase.
A method of isolating from mammalian tissue a DNA sequence encoding ADP-ribosylarginine hydrolase comprising, probing a DNA library prepared from mammalian tissue with an oligonucleotide probe which binds to a conserved portion of the nucleic acid of the rat brain ADP-ribosylarginine hydrolase cDNA within bases 418 to 912 of Seq. I.D. No. 1, wherein said probe is able to detect cDNA encoding ADP-ribosylarginine hydrolase with less than 1% false positives during the probing of the library, and separating any DNA sequence which binds to said probe.
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