Literature DB >> 9036966

Definition of a large region of RAG1 that is important for coimmunoprecipitation of RAG2.

C J McMahan1, M J Sadofsky, D G Schatz.   

Abstract

Interaction between the RAG1 and RAG2 proteins is probably critical for V(D)J recombination. Using a coimmunoprecipitation assay, we define a large region of RAG1 (amino acids 504-1008) that is sufficient for interaction with RAG2. This region comprises the C-terminal half of the RAG1 protein, and is within the region defined as the recombinationally active core. Deletion of either of two regions of RAG1 (amino acids 504-570 or 850-1008) causes a loss of interaction with RAG2. Loss of coimmunoprecipitation is also seen with RAG1 core proteins containing deletions of smaller stretches of amino acids (amino acids 506-511 or 545-550), emphasizing the importance of this region of RAG1 in forming a complex with RAG2. A variety of other small deletion mutations within the amino acid region 504-1008 also decrease coimmunoprecipitation of RAG2 with RAG1, indicating that much or all of this region is important for complex formation.

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Year:  1997        PMID: 9036966

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  18 in total

Review 1.  The RAG proteins in V(D)J recombination: more than just a nuclease.

Authors:  M J Sadofsky
Journal:  Nucleic Acids Res       Date:  2001-04-01       Impact factor: 16.971

2.  A RAG1 and RAG2 tetramer complex is active in cleavage in V(D)J recombination.

Authors:  T Bailin; X Mo; M J Sadofsky
Journal:  Mol Cell Biol       Date:  1999-07       Impact factor: 4.272

3.  Detection of RAG protein-V(D)J recombination signal interactions near the site of DNA cleavage by UV cross-linking.

Authors:  Q M Eastman; I J Villey; D G Schatz
Journal:  Mol Cell Biol       Date:  1999-05       Impact factor: 4.272

Review 4.  RAG1 and RAG2 in V(D)J recombination and transposition.

Authors:  S D Fugmann
Journal:  Immunol Res       Date:  2001       Impact factor: 2.829

5.  Mutational analysis of all conserved basic amino acids in RAG-1 reveals catalytic, step arrest, and joining-deficient mutants in the V(D)J recombinase.

Authors:  Leslie E Huye; Mary M Purugganan; Ming-Ming Jiang; David B Roth
Journal:  Mol Cell Biol       Date:  2002-05       Impact factor: 4.272

6.  A RAG-1/RAG-2 tetramer supports 12/23-regulated synapsis, cleavage, and transposition of V(D)J recombination signals.

Authors:  Patrick C Swanson
Journal:  Mol Cell Biol       Date:  2002-11       Impact factor: 4.272

7.  Overlapping signals for protein degradation and nuclear localization define a role for intrinsic RAG-2 nuclear uptake in dividing cells.

Authors:  Ashley E Ross; Milena Vuica; Stephen Desiderio
Journal:  Mol Cell Biol       Date:  2003-08       Impact factor: 4.272

8.  Identification and characterization of a gain-of-function RAG-1 mutant.

Authors:  Aleksei N Kriatchko; Dirk K Anderson; Patrick C Swanson
Journal:  Mol Cell Biol       Date:  2006-06       Impact factor: 4.272

9.  Footprint analysis of the RAG protein recombination signal sequence complex for V(D)J type recombination.

Authors:  F Nagawa; K Ishiguro; A Tsuboi; T Yoshida; A Ishikawa; T Takemori; A J Otsuka; H Sakano
Journal:  Mol Cell Biol       Date:  1998-01       Impact factor: 4.272

10.  A basic motif in the N-terminal region of RAG1 enhances V(D)J recombination activity.

Authors:  C J McMahan; M J Difilippantonio; N Rao; E Spanopoulou; D G Schatz
Journal:  Mol Cell Biol       Date:  1997-08       Impact factor: 4.272

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