Ullerich F H
Chromosoma. 1975;50(4):393-419. doi: 10.1007/BF00327076.
Previous investigations have shown the sex determination in the monogenic blowfly Chrysomya rufifacies to be controlled by a cytologically not discernible homogametry-heterogamety mechanism in the female. Female-producing (thelygenic) females are assumed to be heterozygous for a dominant female sex realizer (F') with sex-predetermining properties, while male-producing (arrhenogenic) females as well as males are supposed to be homozygous for the recessive allele (f). In order to identify the genetic sex chromosomes of C. rufifacies among its five pairs of long euchromatic chromosomes (nos. 1-5) plus one pair of small heterochromatic ones (no. 6), all chromosomes were marked by reciprocal translocations induced by X-ray treatment of adult males. The inheritance of thirteen different heteroxygous translocations has been analyzed. All of the translocations (eleven) between two of the four longer chromosomes did not show sex-linked inheritance, thus demonstrating the autosomal character of the chromosomes nos 1, 2, 3 and 4. The same is true for the translocation T6 (2/6). Therefore the small heterochromatic chromosome no. 6, corresponding to the morphlogically differentiated six chromosomes within the amphogenic calliphorid species, remains without sex determining function in the monogenic fly. This could be confirmed by the analysis of monosomic (monosomy-6) and trisomic (trisomy-6) individuals, which resulted from meiotic non-disfunction in T6/+ translocation heterozygotes. Contrary to these translocations, the heteroxygous 5/2 translocation (T14) exhibited sex-linked inheritance: There was but a very low frequency (0,76 per cent) of recombinants resulting from crossing-over between F'/f and the translocation breakage point in theylgenic F1 T14/+females. The sex-linked inheritance of T14 was confirmed by the progeny of a thelygenic F1 T14/+ female crossed to a homozygous T14/T14 translocation male.Among the offspring of that F1 T14/+ female, which had received the translocation from its father, all of the F2 T14/+ females were thelygenic compared to their arrhenogenic T14/T14 sisters. These results prove that the chromosomes of pair no. 5 genetically act as X'X-XX sex chromosomes in C. rufifacies.
先前的研究表明,单基因丽蝇红头丽蝇(Chrysomya rufifacies)的性别决定是由一种在细胞学上无法辨别的雌性同配性别-异配性别机制控制的。产生雌性后代(产雌)的雌性被认为是具有性别预决特性的显性雌性性别决定因子(F')的杂合子,而产生雄性后代(产雄)的雌性以及雄性则被认为是隐性等位基因(f)的纯合子。为了在其五对长常染色体(1-5号)加一对小异染色体(6号)中识别出红头丽蝇的遗传性别染色体,通过对成年雄性进行X射线处理诱导的相互易位标记了所有染色体。分析了13种不同的杂合易位的遗传情况。四个较长染色体中两个之间的所有易位(11种)均未显示出性连锁遗传,从而证明了1、2、3和4号染色体的常染色体特征。易位T6(2/ 6)也是如此。因此,与两性金蝇科物种中形态学上分化的六条染色体相对应的小异染色体6号在单基因丽蝇中没有性别决定功能。这可以通过对单倍体(单体-6)和三倍体(三体-6)个体的分析得到证实,这些个体是由T6/+易位杂合子的减数分裂功能异常产生的。与这些易位相反,杂合的5/2易位(T14)表现出性连锁遗传:在产雌F1 T14/+雌性中,F'/f与易位断点之间发生交换产生的重组体频率非常低(0.7 6%)。产雌F1 T14/+雌性与纯合T14/T14易位雄性杂交的后代证实了T14的性连锁遗传。在该F1 T14/+雌性从其父亲那里获得易位的后代中,所有F2 T14/+雌性与其产雄的T14/T14姐妹相比都是产雌的。这些结果证明,在红头丽蝇中,5号染色体在遗传上起着X'X-XX性染色体的作用。