Belyaeva E S, Koryakov D E, Pokholkova G V, Demakova O V, Zhimulev I F
Institute of Cytology and Genetics of Russian Academy of Sciences, Novosibirsk 630090, Russia.
Chromosoma. 1997 Jul;106(2):124-32. doi: 10.1007/s004120050232.
Classic recessive position effect variegation is related to inactivation of genes juxtaposed to heterochromatin and accompanied by cytologically visible heterochromatization (compaction) of the chromosome region containing these genes. Compaction and gene inactivation occur only in the rearranged homologue. In contrast to this, dominant variegation of the bw gene is known to involve transcriptional silencing in both the cis and trans copy, if they are paired. Our paper describes a cyto- logical approach to understanding this phenomenon. Analysis of salivary gland chromosomes carrying In(2R)bwVDe1 and In(2R)bwVDe2, evoking strong dominant bw variegation, has shown that in the rearranged homologues typical heterochromatization of the bw region and proximal neighbouring bands occurs. Heterochromatization was never observed on a normal homologue paired with a rearranged one. The insertion into the chromosome region 59E in the bwD strain is similar to pericentric heterochromatin. The insertion seems to induce heterochromatization of the neighbouring chromosome region and as a result the material of the insert and the 59E1-2 band join into a single block. When variegation is suppressed, the 59E1-2 band can be seen as a separate structure located proximal to the insert. This occurs in salivary gland polytene chromosomes of XYY males at 29 degrees C and in pseudonurse cell polytene chromosomes of otu11/otu11 females. All bands in the region of the non-rearranged homologue show normal morphology. Thus, although in all strains studied we observed heterochromatization in cis, the homologous regions in trans are not visibly affected.
经典的隐性位置效应斑驳与毗邻异染色质的基因失活有关,并伴随着含有这些基因的染色体区域在细胞学上可见的异染色质化(浓缩)。浓缩和基因失活仅发生在重排的同源染色体上。与此相反,已知bw基因的显性斑驳涉及顺式和反式拷贝(如果它们配对)中的转录沉默。我们的论文描述了一种用于理解这一现象的细胞学方法。对携带In(2R)bwVDe1和In(2R)bwVDe2的唾液腺染色体进行分析,这两种染色体引发强烈的显性bw斑驳,结果表明在重排的同源染色体上,bw区域和近端相邻带出现了典型的异染色质化。在与重排同源染色体配对的正常同源染色体上从未观察到异染色质化。bwD品系中插入染色体区域59E的情况类似于着丝粒周围异染色质。这种插入似乎诱导了相邻染色体区域的异染色质化,结果插入片段的物质与59E1 - 2带连接成一个单一的块。当斑驳被抑制时,59E1 - 2带可被视为位于插入片段近端的一个单独结构。这发生在29摄氏度下XYY雄性的唾液腺多线染色体以及otu11/otu11雌性的假滋养细胞多线染色体中。未重排同源染色体区域的所有带都显示出正常的形态。因此,尽管在所有研究的品系中我们都观察到了顺式异染色质化,但反式同源区域并未受到明显影响。