Casanova J, Sánchez-Herrero E, Morata G
J Embryol Exp Morphol. 1985 Dec;90:179-96.
Cbx1 is a dominant mutation of the bithorax complex (BX-C) of Drosophila partially transforming the second thoracic (T2) segment towards the third one (T3). Molecular analysis has shown that Cbx1 arose from a transposition within the BX-C of a DNA fragment of 17 kb containing pbx+ inserted into the Ubx area. In addition to the dominant phenotype, the Cbx1 mutation produces a set of recessive homeotic transformations that we show are characteristic of the Ubx mutations. We present evidence that the dominant and the recessive transformations arise from different mechanisms and suggest the dominant transformation is caused by an alteration of the normal regulatory role of pbx+ resulting in an adventitious expression of some Ubx+ products in T2, while the Ubx phenotype is caused by the breakpoint of the insertion.
Cbx1是果蝇双胸复合体(BX-C)的一个显性突变,它使第二胸节(T2)部分地向第三胸节(T3)转变。分子分析表明,Cbx1起源于一个17 kb DNA片段在BX-C内的转座,该片段包含插入Ubx区域的pbx+。除了显性表型外,Cbx1突变还产生了一组隐性同源异形转变,我们证明这些转变是Ubx突变的特征。我们提供的证据表明,显性和隐性转变源于不同的机制,并表明显性转变是由pbx+正常调控作用的改变引起的,导致T2中一些Ubx+产物的异常表达,而Ubx表型是由插入的断点引起的。