Literature DB >> 16244873

The neurobeachin gene spans the common fragile site FRA13A.

Larissa Savelyeva1, Evgeny Sagulenko, Jens Guido Schmitt, Manfred Schwab.   

Abstract

Common fragile sites are normal constituents of chromosomal structure prone to chromosomal breakage. In humans, the cytogenetic locations of more than 80 common fragile sites are known. The DNA at 11 of them has been defined and characterized at the molecular level. According to the Genome Database, the common fragile site FRA13A maps to chromosome band 13q13.2. Here, we identify the precise genomic position of FRA13A, and characterize the genetic complexity of the fragile DNA sequence. We show that FRA13A breaks are limited to a 650 kb region within the neurobeachin (NBEA) gene, which genomically spans approximately 730 kb. NBEA encodes a neuron-specific multidomain protein implicated in membrane trafficking that is predominantly expressed in the brain and during development.

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Year:  2005        PMID: 16244873     DOI: 10.1007/s00439-005-0083-z

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  42 in total

Review 1.  Common fragile sites.

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2.  The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

Authors:  D Castermans; V Wilquet; E Parthoens; C Huysmans; J Steyaert; L Swinnen; J-P Fryns; W Van de Ven; K Devriendt
Journal:  J Med Genet       Date:  2003-05       Impact factor: 6.318

3.  Custom fluorescent-nucleotide synthesis as an alternative method for nucleic acid labeling.

Authors:  O Henegariu; P Bray-Ward; D C Ward
Journal:  Nat Biotechnol       Date:  2000-03       Impact factor: 54.908

4.  Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.

Authors:  F L Boldog; B Waggoner; T W Glover; I Chumakov; D Le Paslier; D Cohen; R M Gemmill; H A Drabkin
Journal:  Genes Chromosomes Cancer       Date:  1994-12       Impact factor: 5.006

5.  Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.

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Review 6.  The clinical significance of fragile sites on human chromosomes.

Authors:  G R Sutherland; E Baker
Journal:  Clin Genet       Date:  2000-09       Impact factor: 4.438

7.  BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function.

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8.  DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.

Authors:  T W Glover; C Berger; J Coyle; B Echo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer.

Authors:  Stacy R Denison; Gwen Callahan; Nicole A Becker; Leslie A Phillips; David I Smith
Journal:  Genes Chromosomes Cancer       Date:  2003-09       Impact factor: 5.006

10.  Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer.

Authors:  Lorène Rozier; Eliane El-Achkar; Françoise Apiou; Michelle Debatisse
Journal:  Oncogene       Date:  2004-09-09       Impact factor: 9.867

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  24 in total

1.  Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats.

Authors:  Lena M Brueckner; Evgeny Sagulenko; Elisa M Hess; Diana Zheglo; Anne Blumrich; Manfred Schwab; Larissa Savelyeva
Journal:  Hum Genet       Date:  2012-04-05       Impact factor: 4.132

2.  Monozygotic twins with discordant karyotypes following preimplantation genetic screening and single embryo transfer: case report.

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Journal:  J Assist Reprod Genet       Date:  2010-08-11       Impact factor: 3.412

3.  Drosophila mutants of the autism candidate gene neurobeachin (rugose) exhibit neuro-developmental disorders, aberrant synaptic properties, altered locomotion, and impaired adult social behavior and activity patterns.

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Journal:  J Neurogenet       Date:  2015-07-14       Impact factor: 1.250

Review 4.  Molecular characterization of common fragile sites as a strategy to discover cancer susceptibility genes.

Authors:  Larissa Savelyeva; Lena M Brueckner
Journal:  Cell Mol Life Sci       Date:  2014-09-18       Impact factor: 9.261

Review 5.  Fragility Extraordinaire: Unsolved Mysteries of Chromosome Fragile Sites.

Authors:  Wenyi Feng; Arijita Chakraborty
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622

Review 6.  WWOX, large common fragile site genes, and cancer.

Authors:  Ge Gao; David I Smith
Journal:  Exp Biol Med (Maywood)       Date:  2015-01-16

Review 7.  Drosophila Studies on Autism Spectrum Disorders.

Authors:  Yao Tian; Zi Chao Zhang; Junhai Han
Journal:  Neurosci Bull       Date:  2017-08-09       Impact factor: 5.203

8.  Ilex kudingcha C.J. Tseng Mitigates Phenotypic Characteristics of Human Autism Spectrum Disorders in a Drosophila Melanogaster Rugose Mutant.

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9.  Neurobeachin (NBEA) is a target of recurrent interstitial deletions at 13q13 in patients with MGUS and multiple myeloma.

Authors:  Julie O'Neal; Feng Gao; Anjum Hassan; Ryan Monahan; Samantha Barrios; Manfred W Kilimann; Ian Lee; Wee J Chng; Ravi Vij; Michael H Tomasson
Journal:  Exp Hematol       Date:  2009-02       Impact factor: 3.084

Review 10.  Very large common fragile site genes and their potential role in cancer development.

Authors:  Ge Gao; David I Smith
Journal:  Cell Mol Life Sci       Date:  2014-10-10       Impact factor: 9.261

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