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Nonoverlapping functions of DNA polymerases mu, lambda, and terminal deoxynucleotidyltransferase during immunoglobulin V(D)J recombination in vivo.
Bertocci B., De Smet A., Weill J.-C., Reynaud C.-A.
Immunity 25, 1 (2006) 31-41 - http://www.hal.inserm.fr/inserm-00319559
(16860755)
Nonoverlapping functions of DNA polymerases mu, lambda, and terminal deoxynucleotidyltransferase during immunoglobulin V(D)J recombination in vivo.
Barbara Bertocci1, Annie De Smet1, Jean-Claude Weill () 1, Claude-Agnès Reynaud () 1
1:  Developpement du Systeme Immunitaire
INSERM : U783 – Université Paris V - Paris Descartes
Fac de Medecine Necker-Enfants Malades PARIS V 156, Rue de Vaugirard 75730 PARIS CEDEX 15
France
DNA polymerases mu (pol mu), lambda (pol lambda), and terminal deoxynucleotidyltransferase (TdT) are enzymes of the pol X family that share homology in sequence and functional domain organization. We showed previously that pol mu participates in light chain but surprisingly not heavy chain gene rearrangement. We show here that immunoglobulin heavy chain junctions from pol lambda-deficient animals have shorter length with normal N-additions, thus indicating that pol lambda is recruited during heavy chain rearrangement at a step that precedes the action of TdT. In contrast to previous in vitro studies, analysis of animals with combined inactivation of these enzymes revealed no overlapping or compensatory activities for V(D)J recombination between pol mu, pol lambda, and TdT. This complex usage of polymerases with distinct catalytic specificities may correspond to the specific function that the third hypervariable region assumes for each immunoglobulin chain, with pol lambda maintaining a large heavy chain junctional heterogeneity and pol mu ensuring a restricted light chain junctional variability.
Life Sciences/Immunology
English
1074-7613

Article in peer-reviewed journal
10.1016/j.immuni.2006.04.013
Immunity (Immunity)
Publisher Elsevier (Cell Press)
ISSN 1074-7613 
international
2006-07
25
1
31-41

Animals – B-Lymphocytes – Base Sequence – Cell Aging – Cell Differentiation – Cells – Cultured – DNA Nucleotidylexotransferase – DNA Polymerase beta – DNA-Directed DNA Polymerase – Fibroblasts – Gene Expression Regulation – Gene Rearrangement – B-Lymphocyte – Immunoglobulin J-Chains – Immunoglobulin Variable Region – Isoenzymes – Mice – Knockout – RNA Splicing – Recombination – Genetic – Sequence Alignment
A.C.I. "Biologie du Développement et Physiologie Intégrative"du Ministère de la Recherche. Fondation Princesse Grace de Monaco.
Attached file list to this document: 
DOC
Summary.doc(21.5 KB)
manuscript.doc(189 KB)
Table_1.doc(24.5 KB)
Table_2.doc(32 KB)
Table_3.doc(23.5 KB)
ANNEX
BertocciSupplemental_dataset.doc(83.5 KB)
PDF
Bertocci1.pdf(56.2 KB)
Bertocci2.pdf(52.2 KB)
Bertocci3.pdf(43.6 KB)
Bertocci4.pdf(52.3 KB)
Summary.pdf(56.5 KB)
manuscript.pdf(207.6 KB)
Table_1.pdf(31.7 KB)
Table_2.pdf(33.7 KB)
Table_3.pdf(31.8 KB)

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