The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11 -> q13

Citation
K. Buiting et al., The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11 -> q13, CYTOG C GEN, 87(1-2), 1999, pp. 125-131
Citations number
16
Categorie Soggetti
Molecular Biology & Genetics
Journal title
CYTOGENETICS AND CELL GENETICS
ISSN journal
03010171 → ACNP
Volume
87
Issue
1-2
Year of publication
1999
Pages
125 - 131
Database
ISI
SICI code
0301-0171(1999)87:1-2<125:THGFTP>2.0.ZU;2-B
Abstract
The deadenylation nuclease or poly(A)-specific ribonuclease (PARN) is a 3' exonuclease, which degrades the poly(A)-tail of eukaryotic mRNA molecules. By DNA sequence analysis of cDNA and genomic clones, fluorescence in situ h ybridization, and reverse transcriptase-PCR, we have determined that the ac tive human PARN gene is located in 16p13 and that a truncated copy lacking the 5' end is located in 15q11. The truncated gene maps close to a copy of the D15F37 gene family at the proximal Prader-Willi/Angelman (PWS/AS) delet ion breakpoint region. Other copies of the F37 gene family are located at t he distal PWS/AS deletion breakpoint region and on 16p11.2. Although PARN a nd F37 gene sequences are present on 15q and 16p, our data suggest that the synteny of these loci is the result of independent genetic events. Copyrig ht (C) 1999 S. Karger AG, Basel.