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母体Nanos蛋白调控黑腹果蝇生殖系祖细胞中的合子基因表达。

Maternal Nanos regulates zygotic gene expression in germline progenitors of Drosophila melanogaster.

作者信息

Asaoka M, Sano H, Obara Y, Kobayashi S

机构信息

Institute of Biological Sciences, University of Tsukuba, Tsukuba, Ibaraki 305, Japan.

出版信息

Mech Dev. 1998 Nov;78(1-2):153-8. doi: 10.1016/s0925-4773(98)00164-6.

Abstract

Maternal Nanos (Nos) protein is required for germline development in Drosophila embryos. Here we show that Nos regulates zygotic gene expression in the germline progenitors, or pole cells. In order to probe the gene expression in pole cells, we screened ten enhancer-trap lines which showed beta-gal expression in pole cells. All of these enhancer-trap markers were fully activated in pole cells after their migration to the embryonic gonads. In the pole cells lacking Nos, the expression of nine out of ten enhancer-trap markers was affected. Among nine markers, five (Type-A) were prematurely expressed in the pole cells during the course of their migration. The expression of other four markers (Type-B) initiated correctly after pole-cell migration, but their expression was significantly reduced. Thus, we conclude that the maternal Nos plays a dual role in zygotic gene regulation in pole cells: to define the stages of expression for Type-A markers, and to enhance expression for Type-B markers. Contrary to our results, "Heller and Steinmann-Zwicky (1998)" have recently reported that no premature expression of Type-A markers occurs in the pole cells of embryos derived from nos mutant females. This discrepancy is due to the difference in the nos mutant alleles used for these analyses. We used the much stronger allele, nosBN.

摘要

母体Nanos(Nos)蛋白是果蝇胚胎生殖系发育所必需的。在此我们表明,Nos调节生殖系祖细胞即极细胞中的合子基因表达。为了探究极细胞中的基因表达,我们筛选了10个在极细胞中显示β-半乳糖苷酶表达的增强子陷阱系。所有这些增强子陷阱标记在迁移到胚胎性腺后在极细胞中被完全激活。在缺乏Nos的极细胞中,10个增强子陷阱标记中有9个的表达受到影响。在这9个标记中,有5个(A型)在极细胞迁移过程中过早表达。其他4个标记(B型)在极细胞迁移后正确起始表达,但表达显著降低。因此,我们得出结论,母体Nos在极细胞的合子基因调控中起双重作用:确定A型标记的表达阶段,并增强B型标记的表达。与我们的结果相反,“Heller和Steinmann-Zwicky(1998)”最近报道,在源自nos突变雌性的胚胎的极细胞中,A型标记没有过早表达。这种差异是由于用于这些分析的nos突变等位基因不同所致。我们使用的是更强的等位基因nosBN。

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