Literature DB >> 1735560

The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice.

M A Oettinger1, B Stanger, D G Schatz, T Glaser, K Call, D Housman, D Baltimore.   

Abstract

The recombination activating genes RAG-1 and RAG-2 are adjacent genes that act synergistically to activate variable-diversity-joining (V(D)J) recombination. Southern analysis of hybrid cell lines derived from patients with the Wilms tumor-aniridia-genitourinary defects-mental retardation (WAGR) syndrome and from mutagenized cell hybrids selected for deletions in chromosome 11 has allowed us to map the chromosomal location of the human RAG locus. The RAG locus defines a new interval of human chromosome 11p, but is not associated with any genetically mapped human disease. Guided by the chromosomal localization of the human recombination activating genes, we have also mapped the location of the mouse Rag locus.

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Year:  1992        PMID: 1735560     DOI: 10.1007/bf00189518

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  14 in total

1.  Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomes.

Authors:  T G Lugo; B Handelin; A M Killary; D E Housman; R E Fournier
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

2.  The mouse mutation severe combined immune deficiency (scid) is on chromosome 16.

Authors:  G C Bosma; M T Davisson; N R Ruetsch; H O Sweet; L D Shultz; M J Bosma
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

3.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

4.  The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.

Authors:  T Glaser; W H Lewis; G A Bruns; P C Watkins; C E Rogler; T B Shows; V E Powers; H F Willard; J M Goguen; K O Simola
Journal:  Nature       Date:  1986 Jun 26-Jul 2       Impact factor: 49.962

5.  A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.

Authors:  T Glaser; D Housman; W H Lewis; D Gerhard; C Jones
Journal:  Somat Cell Mol Genet       Date:  1989-11

6.  The V(D)J recombination activating gene, RAG-1.

Authors:  D G Schatz; M A Oettinger; D Baltimore
Journal:  Cell       Date:  1989-12-22       Impact factor: 41.582

7.  Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.

Authors:  U Francke; L B Holmes; L Atkins; V M Riccardi
Journal:  Cytogenet Cell Genet       Date:  1979

8.  A severe combined immunodeficiency mutation in the mouse.

Authors:  G C Bosma; R P Custer; M J Bosma
Journal:  Nature       Date:  1983-02-10       Impact factor: 49.962

9.  Selective expression of RAG-2 in chicken B cells undergoing immunoglobulin gene conversion.

Authors:  L M Carlson; M A Oettinger; D G Schatz; E L Masteller; E A Hurley; W T McCormack; D Baltimore; C B Thompson
Journal:  Cell       Date:  1991-01-11       Impact factor: 41.582

10.  Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10.

Authors:  M H Brilliant; G Szabo; Z Katarova; C A Kozak; T M Glaser; R J Greenspan; D E Housman
Journal:  Genomics       Date:  1990-01       Impact factor: 5.736

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  9 in total

Review 1.  Mouse chromosome 2.

Authors:  L D Siracusa; C M Abbott
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.

Authors:  L Li; D Drayna; D Hu; A Hayward; S Gahagan; H Pabst; M J Cowan
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

3.  Omenn's Syndrome: A rare primary immunodeficiency disorder.

Authors:  Ibtisam B Elnour; Shakeel Ahmed; Kamal Halim; V Nirmala
Journal:  Sultan Qaboos Univ Med J       Date:  2007-08

4.  Genes associated with immunoglobulin V(D)J recombination are linked on mouse chromosome 2 and human chromosome 11.

Authors:  K Huppi; D Siwarski; J Shaughnessy; M J Klemsz; M Shirakata; R Maki; H Sakano
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

Review 5.  Role of recombination activating genes in the generation of antigen receptor diversity and beyond.

Authors:  Mayilaadumveettil Nishana; Sathees C Raghavan
Journal:  Immunology       Date:  2012-12       Impact factor: 7.397

6.  Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13.

Authors:  K Schwarz; H Hameister; M Gessler; K H Grzeschik; T E Hansen-Hagge; C R Bartram
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

Review 7.  Omenn syndrome: a disorder of Rag1 and Rag2 genes.

Authors:  A Villa; S Santagata; F Bozzi; L Imberti; L D Notarangelo
Journal:  J Clin Immunol       Date:  1999-03       Impact factor: 8.317

8.  The value of family history in diagnosing primary immunodeficiency disorders.

Authors:  Mohamed A Hendaus; Ahmad Alhammadi; Mehdi M Adeli; Fawzia Al-Yafei
Journal:  Case Rep Pediatr       Date:  2014-08-05

9.  NOD-Rag2null IL-2Rγnull mice: an alternative to NOG mice for generation of humanized mice.

Authors:  Ikumi Katano; Ryoji Ito; Tsutomu Kamisako; Tomoo Eto; Tomoyuki Ogura; Kenji Kawai; Hiroshi Suemizu; Takeshi Takahashi; Yutaka Kawakami; Mamoru Ito
Journal:  Exp Anim       Date:  2014
  9 in total

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