• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

果蝇胚胎中存在两种极细胞,一种对第三个P因子内含子具有剪接活性,另一种则没有。

Two types of pole cells are present in the Drosophila embryo, one with and one without splicing activity for the third P-element intron.

作者信息

Kobayashi S, Kitamura T, Sasaki H, Okada M

机构信息

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

出版信息

Development. 1993 Mar;117(3):885-93. doi: 10.1242/dev.117.3.885.

DOI:10.1242/dev.117.3.885
PMID:8391978
Abstract

In Drosophila, it has been postulated that the third intron of the P-element is spliced only in germ-line cells. To test whether this postulate is applicable to pole cells, the progenitor cells of germ line, we carried out a histochemical assay to detect the splicing activity in embryos. The splicing activity was detected in pole cells and primordial germ cells. The activity increased to reach a maximum at 5-6 hours AEL (after egg laying), then decreased to an undetectable level by 8-9 hours AEL. The splicing activity showed a small second peak at 12-15 hours AEL. It was rather unexpected that not all pole cells were capable of splicing the third intron. Almost all pole cells that had the splicing activity at 5-6 hours AEL penetrated the embryonic gonads and differentiated into primordial germ cells. Our findings suggest that pole cells are selected to penetrate the gonads while they are migrating from the proctodeal cavity to the gonads. Furthermore, these results suggest that the machinery to splice the P-element is active in some pole cells, and that this activity is used for processing transcripts of genes that play important roles in the differentiation of pole cells into primordial germ cells.

摘要

在果蝇中,有人推测P因子的第三个内含子仅在生殖系细胞中进行剪接。为了测试这一推测是否适用于极细胞(生殖系的祖细胞),我们进行了一项组织化学检测以检测胚胎中的剪接活性。在极细胞和原始生殖细胞中检测到了剪接活性。该活性在产卵后(AEL)5 - 6小时增加到最大值,然后在8 - 9小时AEL时降至检测不到的水平。剪接活性在12 - 15小时AEL时出现一个较小的第二个峰值。并非所有极细胞都能够剪接第三个内含子,这相当出人意料。几乎所有在5 - 6小时AEL具有剪接活性的极细胞都会穿透胚胎性腺并分化为原始生殖细胞。我们的研究结果表明,极细胞在从原肛腔迁移到性腺的过程中被选择穿透性腺。此外,这些结果表明,剪接P因子的机制在一些极细胞中是活跃的,并且这种活性用于处理在极细胞分化为原始生殖细胞过程中起重要作用的基因的转录本。

相似文献

1
Two types of pole cells are present in the Drosophila embryo, one with and one without splicing activity for the third P-element intron.果蝇胚胎中存在两种极细胞,一种对第三个P因子内含子具有剪接活性,另一种则没有。
Development. 1993 Mar;117(3):885-93. doi: 10.1242/dev.117.3.885.
2
Identification of a cis-acting sequence required for germ line-specific splicing of the P element ORF2-ORF3 intron.P元件ORF2-ORF3内含子生殖系特异性剪接所需的顺式作用序列的鉴定。
Mol Cell Biol. 1991 Mar;11(3):1538-46. doi: 10.1128/mcb.11.3.1538-1546.1991.
3
Developmentally Regulated Splicing of the Third Intron of P Element in Somatic Tissues in Drosophila Embryos: (transposon/P element/splicing/Drosophila embryo).果蝇胚胎体细胞组织中P因子第三个内含子的发育调控剪接:(转座子/P因子/剪接/果蝇胚胎)
Dev Growth Differ. 1993 Feb;35(1):67-73. doi: 10.1111/j.1440-169X.1993.00067.x.
4
Analysis of the cis-acting requirements for germ-line-specific splicing of the P-element ORF2-ORF3 intron.
Genes Dev. 1989 May;3(5):720-8. doi: 10.1101/gad.3.5.720.
5
Induction of indora expression in pole cells by the mesoderm is required for female germ-line development in Drosophila melanogaster.中胚层诱导极细胞中indora表达是黑腹果蝇雌性生殖系发育所必需的。
Development. 1999 Feb;126(5):1023-9. doi: 10.1242/dev.126.5.1023.
6
Transplantation of posterior polar plasm in Drosophila. Induction of germ cells at the anterior pole of the egg.果蝇后极质的移植。卵前极生殖细胞的诱导。
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1016-20. doi: 10.1073/pnas.71.4.1016.
7
P element-mediated germ-line transformation of Drosophila.P 因子介导的果蝇种系转化
Methods Mol Biol. 1993;18:75-85. doi: 10.1385/0-89603-245-0:75.
8
A test for enhancement of cytotype regulation in Drosophila melanogaster by the transposase-encoding P element ∆2-3.转座酶编码 P 元件 ∆2-3 增强果蝇细胞型调控的检测。
Mol Genet Genomics. 2013 Oct;288(10):535-47. doi: 10.1007/s00438-013-0772-6. Epub 2013 Aug 8.
9
Migration of primordial germ cells isolated from embryonic blood into the gonads after transfer to stage X blastoderms and detection of germline chimaerism by PCR.从胚胎血液中分离出的原始生殖细胞转移至X期胚盘后向性腺迁移,并通过聚合酶链反应检测种系嵌合体。
Br Poult Sci. 2004 Dec;45(6):762-8. doi: 10.1080/00071660400014325.
10
The mechanism of somatic inhibition of Drosophila P-element pre-mRNA splicing: multiprotein complexes at an exon pseudo-5' splice site control U1 snRNP binding.果蝇P因子前体mRNA剪接的体细胞抑制机制:外显子假5'剪接位点处的多蛋白复合物控制U1 snRNP结合。
Genes Dev. 1992 Aug;6(8):1386-401. doi: 10.1101/gad.6.8.1386.

引用本文的文献

1
Regional expression of the transcript encoding sterol carrier protein x-related thiolase and its regulation by homeotic genes in the midgut of Drosophila embryos.果蝇胚胎中肠中编码固醇载体蛋白X相关硫解酶的转录本的区域表达及其受同源异型基因的调控。
Dev Growth Differ. 1996 Aug;38(4):373-381. doi: 10.1046/j.1440-169X.1996.t01-3-00005.x.
2
Nanos suppresses somatic cell fate in Drosophila germ line.Nanos抑制果蝇生殖系中的体细胞命运。
Proc Natl Acad Sci U S A. 2004 Jul 13;101(28):10338-42. doi: 10.1073/pnas.0401647101. Epub 2004 Jul 6.
3
A small family of elements with long inverted repeats is located near sites of developmentally regulated DNA rearrangement in Tetrahymena thermophila.
在嗜热四膜虫中,一小类具有长反向重复序列的元件位于发育调控的DNA重排位点附近。
Mol Cell Biol. 1994 Sep;14(9):5939-49. doi: 10.1128/mcb.14.9.5939-5949.1994.