Dorf M E, Stimpfling J H, Benacerraf B
J Immunol. 1979 Jul;123(1):269-71.
(B10.A x B10.S)F1 hybrid mice produce lower levels of anti-GL phi antibody than B10.S(9R) and B10.HTT mice. To determine whether this difference is due to a gene dose or a cis-trans effect, [B10.S(9R) x B10.S(8R)]F1 mice were immunized with GL phi. These mice carry one dose of the responder Ir gene alleles in the cis position whereas the recombinant B10.S(9R) and B10.HTT mice carry two doses of the relevant genes. Both (B10.A x B10.S) and [B10.S(9R) x B10.S(8R)] F1 mice produced comparably lower amounts of antibodies as compared to the recombinant strains. The data therefore demonstrate that gene dose and not cis-trans effect accounts for the differences between F1 and recombinant strains in their antibody response to GL phi controlled by complementary Ir genes.
(B10.A×B10.S)F1杂种小鼠产生的抗GL phi抗体水平低于B10.S(9R)和B10.HTT小鼠。为了确定这种差异是由于基因剂量还是顺式-反式效应,用GL phi免疫[B10.S(9R)×B10.S(8R)]F1小鼠。这些小鼠在顺式位置携带一剂反应性Ir基因等位基因,而重组B10.S(9R)和B10.HTT小鼠携带两剂相关基因。与重组品系相比,(B10.A×B10.S)和[B10.S(9R)×B10.S(8R)]F1小鼠产生的抗体量相对较低。因此,数据表明,在对由互补Ir基因控制的GL phi的抗体反应中,是基因剂量而非顺式-反式效应导致了F1品系和重组品系之间的差异。