Gorry P, Lufkin T, Dierich A, Rochette-Egly C, Décimo D, Dollé P, Mark M, Durand B, Chambon P
Laboratoire de Génétique Moléculaire des Eucaryotes du Centre National de la Recherche Scientifique, Strasbourg, France.
Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9032-6. doi: 10.1073/pnas.91.19.9032.
The cellular retinoic acid binding proteins I and II (CRABPI and CRABPII) bind retinoic acid with high affinity, exhibit distinct patterns of expression during embryonic development, and are thought to play important roles in the RA signaling pathway. We have generated a targeted mutation of the CRABPI gene using the "hit-and-run" strategy and shown that it prevents the production of a functional CRABPI protein. Homozygous mutant mice were normal, indicating that CRABPI does not play a crucial role in the RA signaling pathway.
细胞视黄酸结合蛋白I和II(CRABPI和CRABPII)以高亲和力结合视黄酸,在胚胎发育过程中表现出不同的表达模式,并被认为在视黄酸(RA)信号通路中发挥重要作用。我们使用“打了就跑”策略产生了CRABPI基因的靶向突变,并表明它阻止了功能性CRABPI蛋白的产生。纯合突变小鼠是正常的,这表明CRABPI在RA信号通路中不发挥关键作用。