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Genomic organization of the UBE3A/E6-AP gene and related pseudogenes.

作者信息

Kishino T, Wagstaff J

机构信息

Genetics Division, Children's Hospital, Boston, Massachusetts, USA.

出版信息

Genomics. 1998 Jan 1;47(1):101-7. doi: 10.1006/geno.1997.5093.

DOI:10.1006/geno.1997.5093
PMID:9465301
Abstract

The UBE3A gene encodes the E6-AP ubiquitin-protein ligase and has recently been shown to be mutated in Angelman syndrome patients who lack 15q11-q13 deletions or chromosome 15 paternal uniparental disomy. Previous UBE3A cDNA analysis has shown a coding region of approximately 2.6 kb and a 3'-untranslated region (UTR) of < 50 bp, whereas Northern analysis has indicated mRNA sizes of 5-8 kb. We have analyzed additional cDNA clones and provide evidence for an additional 0.5 kb of 5'-UTR and > 2 kb of 3'-UTR. We have established the genomic organization of UBE3A and the sequence of intron-exon borders. We have also mapped two highly homologous processed pseudogenes, UBE3AP1 and UBE3AP2, to chromosomes 2 and 21, respectively, and determined their genomic organization. These results will form the basis for studies of mutation and imprinting of UBE3A.

摘要

相似文献

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Genomic organization of the UBE3A/E6-AP gene and related pseudogenes.
Genomics. 1998 Jan 1;47(1):101-7. doi: 10.1006/geno.1997.5093.
2
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UBE3A/E6-AP mutations cause Angelman syndrome.UBE3A/E6-AP突变导致天使综合征。
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