Bertocci Barbara, De Smet Annie, Flatter Eric, Dahan Auriel, Bories Jean-Christophe, Landreau Catherine, Weill Jean-Claude, Reynaud Claude-Agnès
Institut National de la Santé et de la Recherche Médicale, Unité 373, Faculté de Médecine Necker-Enfants Malades, Paris, France.
J Immunol. 2002 Apr 15;168(8):3702-6. doi: 10.4049/jimmunol.168.8.3702.
Mutations arising in Ig V genes during an immune response are most likely introduced by one or several error-prone DNA polymerases. Many of the recently described nonreplicative DNA polymerases have an intrinsic fidelity compatible with such an activity, the strongest candidates being polymerase (pol) eta, pol iota, pol zeta, and pol mu. We report in this work that mice inactivated for either of the two polymerases related to pol beta (i.e., pol mu and pol lambda) are viable and fertile and display a normal hypermutation pattern.
免疫反应过程中Ig V基因产生的突变很可能是由一种或几种易出错的DNA聚合酶引入的。最近描述的许多非复制性DNA聚合酶具有与这种活性相匹配的内在保真度,最有可能的候选者是聚合酶(pol)η、pol ι、pol ζ和pol μ。我们在这项研究中报告,与pol β相关的两种聚合酶(即pol μ和pol λ)中任何一种失活的小鼠都是有活力且可育的,并且表现出正常的高突变模式。