Naruse I, Kameyama Y
Teratology. 1986 Dec;34(3):283-9. doi: 10.1002/tera.1420340308.
Male mice heterozygous for the dominant polydactyly gene Pdn (Polydactyly Nagoya) were crossed with normal or heterozygous females of the same strain. Pregnant females were treated with 5 mg/kg of cytosine arabinoside (Ara-C) on day 12 of gestation. The offspring were removed on day 18 of gestation and examined for external malformations, and the fore- and hindlimbs were examined by means of bone- and cartilage-stained cleared specimens. In +/+ x Pdn/+ matings, Pdn/+ fetuses, bearing preaxial polydactyly of the distal phalangeal type in the hindlimb and deformity of the 1st digit in the forelimb, were obtained in about 50% of the nontreated group. In treated fetuses, however, the incidence of polydactyly and deformity of the 1st digit decreased to 1.4 and 10.1%, respectively. Nontreated Pdn/Pdn fetuses exhibited preaxial polydactyly of the duplicated or triplicated metacarpal/metatarsal type both in the fore- and hindlimbs. In the treated Pdn/Pdn fetuses, the number of preaxial extra digits decreased in both limbs. Some hindlimbs of the treated Pdn/Pdn fetuses exhibited five metatarsals, normally. In the vitally stained specimens at 6 and 24 hours after injection of Ara-C, preaxial marginal necrotic zones (fMI) were observed in almost all of the treated embryos from +/+ x Pdn/+ matings. However, approximately half of the embryos did not exhibit fMI in the nontreated control group at the same stage. Those embryos deficient in fMI were regarded as Pdn/+. These findings indicated that a subteratogenic dose of Ara-C prevented the genetic expression of polydactyly in almost all Pdn/+ and some cases of Pdn/Pdn mice.(ABSTRACT TRUNCATED AT 250 WORDS)
携带显性多指基因Pdn(名古屋多指)的杂合子雄性小鼠与同品系的正常或杂合子雌性小鼠杂交。怀孕雌性小鼠在妊娠第12天接受5mg/kg的阿糖胞苷(Ara-C)处理。在妊娠第18天取出后代,检查其外部畸形情况,并通过骨和软骨染色的透明标本检查前肢和后肢。在+/+×Pdn/+交配中,在未处理组中约50%的Pdn/+胎儿出现后肢远节指骨型轴前多指以及前肢第1指畸形。然而,在经处理的胎儿中,多指和第1指畸形的发生率分别降至1.4%和10.1%。未处理的Pdn/Pdn胎儿在前肢和后肢均表现出重复或三联掌骨/跖骨型轴前多指。在经处理的Pdn/Pdn胎儿中,两肢的轴前额外指数量均减少。经处理的Pdn/Pdn胎儿的一些后肢通常有5根跖骨。在注射Ara-C后6小时和24小时的活体染色标本中,在几乎所有来自+/+×Pdn/+交配的经处理胚胎中均观察到轴前边缘坏死区(fMI)。然而,在同一阶段的未处理对照组中,约一半的胚胎未表现出fMI。那些缺乏fMI的胚胎被视为Pdn/+。这些发现表明,亚致畸剂量的Ara-C几乎可阻止所有Pdn/+以及部分Pdn/Pdn小鼠中多指的基因表达。(摘要截短至250字)