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意外发现δ,一种果蝇锌指蛋白,在合子基因转录开始时存在于胚胎细胞核中。

Serendipity delta, a Drosophila zinc finger protein present in embryonic nuclei at the onset of zygotic gene transcription.

作者信息

Payre F, Yanicostas C, Vincent A

机构信息

Centre de Recherches de Biologie et Génétique Cellulaires du CNRS, Toulouse, France.

出版信息

Dev Biol. 1989 Dec;136(2):469-80. doi: 10.1016/0012-1606(89)90272-8.

DOI:10.1016/0012-1606(89)90272-8
PMID:2511050
Abstract

Serendipity delta (sry delta) is a member of a set of Drosophila zinc finger protein genes showing maximal transcription during oogenesis. By using transformant lines, we monitored the zygotic expression of the sry delta gene and characterized some biochemical properties of a sry delta/beta-galactosidase fusion protein-containing fingers. Further analysis made use of anti-sry delta specific antibodies. During oogenesis, while sry delta mRNAs transcribed by nurse cells are transferred to the oocyte starting in stage 10, translation into protein occurs in the ooplasm starting in stage 12. The maternally inherited protein concentrates in embryonic nuclei during early cleavages, prior to the onset of zygotic transcription. At the blastoderm stage, the sry delta protein is localized in all somatic nuclei. Later in embryogenesis and up to the adult stage, the zygotic protein is present in nuclei of transcriptionally active cells (both somatic and germ line). These data are consistent with the sry delta protein being a transcription factor, with a role in zygotic activation of general cellular functions.

摘要

意外发现δ(sryδ)是一组果蝇锌指蛋白基因的成员,在卵子发生过程中表现出最大转录水平。通过使用转化株系,我们监测了sryδ基因的合子表达,并对含sryδ/β-半乳糖苷酶融合蛋白的锌指的一些生化特性进行了表征。进一步的分析利用了抗sryδ特异性抗体。在卵子发生过程中,虽然由滋养细胞转录的sryδ mRNA从第10阶段开始转移到卵母细胞中,但蛋白质的翻译从第12阶段开始在卵质中发生。母系遗传的蛋白质在合子转录开始之前的早期卵裂过程中集中在胚胎细胞核中。在囊胚期,sryδ蛋白定位于所有体细胞核中。在胚胎发育后期直至成虫阶段,合子蛋白存在于转录活跃细胞(体细胞和生殖细胞系)的细胞核中。这些数据与sryδ蛋白作为一种转录因子一致,在合子激活一般细胞功能中发挥作用。

相似文献

1
Serendipity delta, a Drosophila zinc finger protein present in embryonic nuclei at the onset of zygotic gene transcription.意外发现δ,一种果蝇锌指蛋白,在合子基因转录开始时存在于胚胎细胞核中。
Dev Biol. 1989 Dec;136(2):469-80. doi: 10.1016/0012-1606(89)90272-8.
2
The closely related Drosophila sry beta and sry delta zinc finger proteins show differential embryonic expression and distinct patterns of binding sites on polytene chromosomes.密切相关的果蝇sry beta和sry delta锌指蛋白在胚胎期表达不同,在多线染色体上的结合位点模式也不同。
Development. 1990 Sep;110(1):141-9. doi: 10.1242/dev.110.1.141.
3
sry h-1, a new Drosophila melanogaster multifingered protein gene showing maternal and zygotic expression.sry h-1,一个新的黑腹果蝇多指蛋白基因,呈现母体和合子表达。
Mol Cell Biol. 1988 Oct;8(10):4459-68. doi: 10.1128/mcb.8.10.4459-4468.1988.
4
Single amino acid exchanges in separate domains of the Drosophila serendipity delta zinc finger protein cause embryonic and sex biased lethality.果蝇意外δ锌指蛋白不同结构域中的单个氨基酸交换会导致胚胎致死和性别偏向性致死。
Genetics. 1992 Aug;131(4):905-16. doi: 10.1093/genetics/131.4.905.
5
Direct control of transcription of the Drosophila morphogen bicoid by the serendipity delta zinc finger protein, as revealed by in vivo analysis of a finger swap.通过手指交换的体内分析揭示,果蝇形态发生素双胸蛋白的转录受意外δ锌指蛋白的直接控制。
Genes Dev. 1994 Nov 15;8(22):2718-28. doi: 10.1101/gad.8.22.2718.
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Sequence and structure of the serendipity locus of Drosophila melanogaster. A densely transcribed region including a blastoderm-specific gene.黑腹果蝇意外基因座的序列与结构。一个包含胚盘特异性基因的高度转录区域。
J Mol Biol. 1985 Nov 5;186(1):149-66. doi: 10.1016/0022-2836(85)90265-7.
7
Two types of zinc fingers are required for dimerization of the serendipity delta transcriptional activator.意外δ转录激活因子二聚化需要两种类型的锌指。
Mol Cell Biol. 1997 Jun;17(6):3137-45. doi: 10.1128/MCB.17.6.3137.
8
Interspecific comparison of Drosophila serendipity delta and beta: multimodular structure of these C2H2 zinc finger proteins.果蝇意外蛋白δ和β的种间比较:这些C2H2锌指蛋白的多模块结构
J Mol Evol. 1994 Mar;38(3):263-73. doi: 10.1007/BF00176088.
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Blastoderm-specific and read-through transcription of the sry alpha gene transformed into the Drosophila genome.转化到果蝇基因组中的sry alpha基因的胚盘特异性转录和通读转录。
Dev Biol. 1986 Dec;118(2):480-7. doi: 10.1016/0012-1606(86)90019-9.
10
Zinc fingers and other domains cooperate in binding of Drosophila sry beta and delta proteins at specific chromosomal sites.锌指结构域和其他结构域协同作用,使果蝇的sryβ和δ蛋白结合于特定染色体位点。
Mol Cell Biol. 1992 Feb;12(2):724-33. doi: 10.1128/mcb.12.2.724-733.1992.

引用本文的文献

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Screens for piwi suppressors in Drosophila identify dosage-dependent regulators of germline stem cell division.在果蝇中筛选piwi抑制因子可鉴定生殖系干细胞分裂的剂量依赖性调节因子。
Genetics. 2003 Dec;165(4):1971-91. doi: 10.1093/genetics/165.4.1971.
2
Two types of zinc fingers are required for dimerization of the serendipity delta transcriptional activator.意外δ转录激活因子二聚化需要两种类型的锌指。
Mol Cell Biol. 1997 Jun;17(6):3137-45. doi: 10.1128/MCB.17.6.3137.
3
Separate cis-regulatory sequences control expression of serendipity beta and janus A, two immediately adjacent Drosophila genes.
独立的顺式调控序列控制着偶然β基因和雅努斯A基因的表达,这两个基因在果蝇中紧邻。
Mol Gen Genet. 1995 Mar 10;246(5):549-60. doi: 10.1007/BF00298961.
4
Transcriptional and translational cis-regulatory sequences of the spermatocyte-specific Drosophila janusB gene are located in the 3' exonic region of the overlapping janusA gene.果蝇精母细胞特异性janusB基因的转录和顺式翻译调控序列位于重叠基因janusA的3'外显子区域。
Mol Gen Genet. 1990 Dec;224(3):450-8. doi: 10.1007/BF00262440.
5
The maternal store of zinc finger protein encoding mRNAs in fully grown Xenopus oocytes is not required for early embryogenesis.在完全成熟的非洲爪蟾卵母细胞中,编码锌指蛋白的mRNA的母体储存对于早期胚胎发育并非必需。
EMBO J. 1991 Jun;10(6):1407-13. doi: 10.1002/j.1460-2075.1991.tb07661.x.
6
Genomic targets of the serendipity beta and delta zinc finger proteins and their respective DNA recognition sites.意外β和δ锌指蛋白的基因组靶点及其各自的DNA识别位点。
EMBO J. 1991 Sep;10(9):2533-41. doi: 10.1002/j.1460-2075.1991.tb07793.x.
7
Zinc fingers and other domains cooperate in binding of Drosophila sry beta and delta proteins at specific chromosomal sites.锌指结构域和其他结构域协同作用,使果蝇的sryβ和δ蛋白结合于特定染色体位点。
Mol Cell Biol. 1992 Feb;12(2):724-33. doi: 10.1128/mcb.12.2.724-733.1992.
8
Single amino acid exchanges in separate domains of the Drosophila serendipity delta zinc finger protein cause embryonic and sex biased lethality.果蝇意外δ锌指蛋白不同结构域中的单个氨基酸交换会导致胚胎致死和性别偏向性致死。
Genetics. 1992 Aug;131(4):905-16. doi: 10.1093/genetics/131.4.905.