Human RNA-specific adenosine deaminase ADAR1 transcripts possess alternative exon 1 structures that initiate from different promoters, one constitutively active and the other interferon inducible

Citation
Cx. George et Ce. Samuel, Human RNA-specific adenosine deaminase ADAR1 transcripts possess alternative exon 1 structures that initiate from different promoters, one constitutively active and the other interferon inducible, P NAS US, 96(8), 1999, pp. 4621-4626
Citations number
40
Categorie Soggetti
Multidisciplinary
Journal title
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN journal
00278424 → ACNP
Volume
96
Issue
8
Year of publication
1999
Pages
4621 - 4626
Database
ISI
SICI code
0027-8424(19990413)96:8<4621:HRADAT>2.0.ZU;2-8
Abstract
RNA-specific adenosine deaminase (ADAR1) catalyzes the deamination of adeno sine to inosine in viral and cellular RNAs. Two size forms of the ADAR1 edi ting enzyme are known, an IPN-inducible approximate to 150-kDa protein and a constitutively expressed N-terminally truncated approximate to 110-kDa pr otein. We have now identified alternative exon 1 structures of human ADAR1 transcripts that initiate from unique promoters, one constitutively express ed and the other IBN inducible. Cloning and sequence analyses of S'-rapid a mplification of cDNA ends (RACE) cDNAs from human placenta established a li nkage between exon 2 of ADAR1 and two alternative exon 1 structures, design ated herein as exon 1A and exon 1B. Analysis of RNA isolated from untreated and IPN-treated human amnion cells demonstrated that exon 1B-exon 2 transc ripts were synthesized in the absence of IBN and were not significantly alt ered in amount by IFN treatment. By contrast, exon 1A-exon 2 transcripts we re IFN inducible. Transient transfection analysis with reporter constructs led to the identification of two functional promoters, designated P-C and P -I. Exon 1B transcripts were initiated from the P-C promoter whose activity in transient transfection reporter assays was not increased by IFN treatme nt. The 107-nt exon 1B mapped 14.5 kb upstream of exon 2, The 201-nt exon 1 A that mapped 5.4 kb upstream of exon 2 was initiated from the interferon-i nducible P-I promoter. These results suggest that two promoters, one IFN in ducible and the other not, initiate transcription of the ADAR1 gene, and th at alternative splicing of unique exon 1 structures to a common exon 2 junc tion generates RNA transcripts with the deduced coding capacity for either the constitutively expressed approximate to 110-kDa ADAR1 protein (exon 1B) or the interferon-induced approximate to 150-kDa ADAR1 protein (exon 1A).