Literature DB >> 8188218

The human gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster in chromosome 15q11-q13 is rich in highly polymorphic (CA)n repeats.

K Glatt1, D Sinnett, M Lalande.   

Abstract

The gamma-aminobutyric acid (GABAA) receptor beta 3 (GABRB3) and alpha 5 (GABRA5) subunit genes have been localized to the Angelman and Prader-Willi syndrome region of chromosome 15q11-q13. GABRB3, which encompasses 250 kb, is located 100 kb proximal of GABRA5, with the two genes arranged in head-to-head transcriptional orientation. In screening 135 kb of cloned DNA within a 260-kb interval extending from within GABRB3 to the 5' end of GABRA5, 10 new (CA)n repeats have been identified. Five of these have been analyzed in detail and found to be highly polymorphic, with the polymorphism information content (PIC) ranging from 0.7 to 0.85 and with heterozygosities of 67 to 94%. In the clones from GABRB3/GABRA5 region, therefore, the frequency of (CA)n with PICs > or = 0.7 is 1 per 27 kb. Previous estimates of the density of (CA)n with PICs > or = 0.7 in the human genome have been approximately 10-fold lower. The GABRB3/GABRA5 region appears, therefore, to be enriched for highly informative (CA)n. This set of closely spaced, short tandem repeat polymorphisms will be useful in the molecular analyses of Prader-Willi and Angelman syndromes and in high-resolution studies of genetic recombination within this region.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8188218     DOI: 10.1006/geno.1994.1027

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  10 in total

Review 1.  Consequences of the evolution of the GABA(A) receptor gene family.

Authors:  Mark G Darlison; Inderjit Pahal; Christian Thode
Journal:  Cell Mol Neurobiol       Date:  2005-06       Impact factor: 5.046

2.  Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Authors:  V Greger; J H Knoll; J Wagstaff; E Woolf; P Lieske; H Glatt; P A Benn; S S Rosengren; M Lalande
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

3.  Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

Authors:  E H Cook; V Lindgren; B L Leventhal; R Courchesne; A Lincoln; C Shulman; C Lord; E Courchesne
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

4.  Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.

Authors:  S L Christian; N K Bhatt; S A Martin; J S Sutcliffe; T Kubota; B Huang; A Mutirangura; A C Chinault; A L Beaudet; D H Ledbetter
Journal:  Genome Res       Date:  1998-02       Impact factor: 9.043

5.  Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.

Authors:  E H Cook; R Y Courchesne; N J Cox; C Lord; D Gonen; S J Guter; A Lincoln; K Nix; R Haas; B L Leventhal; E Courchesne
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

6.  Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.

Authors:  Miyabi Tanaka; Richard W Olsen; Marco T Medina; Emily Schwartz; Maria Elisa Alonso; Reyna M Duron; Ramon Castro-Ortega; Iris E Martinez-Juarez; Ignacio Pascual-Castroviejo; Jesus Machado-Salas; Rene Silva; Julia N Bailey; Dongsheng Bai; Adriana Ochoa; Aurelio Jara-Prado; Gregorio Pineda; Robert L Macdonald; Antonio V Delgado-Escueta
Journal:  Am J Hum Genet       Date:  2008-06       Impact factor: 11.025

7.  Molecular screening for proximal 15q abnormalities in a mentally retarded population.

Authors:  J Jacobsen; B H King; B L Leventhal; S L Christian; D H Ledbetter; E H Cook
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

8.  Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.

Authors:  Andras Szabo; Marta Czako; Kinga Hadzsiev; Balazs Duga; Katalin Komlosi; Bela Melegh
Journal:  Mol Cytogenet       Date:  2015-06-25       Impact factor: 2.009

9.  Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.

Authors:  Yoshiji Yamada; Jun Sakuma; Ichiro Takeuchi; Yoshiki Yasukochi; Kimihiko Kato; Mitsutoshi Oguri; Tetsuo Fujimaki; Hideki Horibe; Masaaki Muramatsu; Motoji Sawabe; Yoshinori Fujiwara; Yu Taniguchi; Shuichi Obuchi; Hisashi Kawai; Shoji Shinkai; Seijiro Mori; Tomio Arai; Masashi Tanaka
Journal:  Int J Mol Med       Date:  2017-05-03       Impact factor: 4.101

10.  Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients.

Authors:  Márta Czakó; Ágnes Till; András Szabó; Réka Ripszám; Béla Melegh; Kinga Hadzsiev
Journal:  Int J Mol Sci       Date:  2019-10-05       Impact factor: 5.923

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.