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本文引用的文献

1
Stages of oocyte development in the zebrafish, Brachydanio rerio.斑马鱼(短担尼鱼)卵母细胞发育阶段
J Morphol. 1993 Nov;218(2):203-224. doi: 10.1002/jmor.1052180209.
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Drosophila Dicer-2 has an RNA interference-independent function that modulates Toll immune signaling.果蝇Dicer-2具有一种独立于RNA干扰的功能,可调节Toll免疫信号传导。
Sci Adv. 2015 Oct 16;1(9):e1500228. doi: 10.1126/sciadv.1500228. eCollection 2015 Oct.
3
Cortical depth and differential transport of vegetally localized dorsal and germ line determinants in the zebrafish embryo.斑马鱼胚胎中植物性定位的背侧和生殖系决定因子的皮质深度及差异运输。
Bioarchitecture. 2014;5(1-2):13-26. doi: 10.1080/19490992.2015.1080891.
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Antisense Oligonucleotide-Mediated Transcript Knockdown in Zebrafish.反义寡核苷酸介导的斑马鱼转录本敲低
PLoS One. 2015 Oct 5;10(10):e0139504. doi: 10.1371/journal.pone.0139504. eCollection 2015.
5
Kinesin-1 interacts with Bucky ball to form germ cells and is required to pattern the zebrafish body axis.驱动蛋白-1与巴基球相互作用形成生殖细胞,并且是斑马鱼体轴模式形成所必需的。
Development. 2015 Sep 1;142(17):2996-3008. doi: 10.1242/dev.124586. Epub 2015 Aug 7.
6
Drosophila germ granules are structured and contain homotypic mRNA clusters.果蝇生殖颗粒具有特定结构并包含同型mRNA簇。
Nat Commun. 2015 Aug 5;6:7962. doi: 10.1038/ncomms8962.
7
Zebrafish germ cells: motility and guided migration.斑马鱼生殖细胞:运动和导向迁移。
Curr Opin Cell Biol. 2015 Oct;36:80-5. doi: 10.1016/j.ceb.2015.07.007. Epub 2015 Jul 31.
8
Genetic compensation induced by deleterious mutations but not gene knockdowns.有害突变而非基因敲低诱导的遗传补偿。
Nature. 2015 Aug 13;524(7564):230-3. doi: 10.1038/nature14580. Epub 2015 Jul 13.
9
Identification of lncRNA MEG3 Binding Protein Using MS2-Tagged RNA Affinity Purification and Mass Spectrometry.利用MS2标记的RNA亲和纯化和质谱技术鉴定lncRNA MEG3结合蛋白
Appl Biochem Biotechnol. 2015 Aug;176(7):1834-45. doi: 10.1007/s12010-015-1680-5. Epub 2015 Jul 9.
10
A functional Bucky ball-GFP transgene visualizes germ plasm in living zebrafish.一种功能性巴基球-绿色荧光蛋白转基因在活斑马鱼中使生殖质可视化。
Gene Expr Patterns. 2015 May-Jul;18(1-2):44-52. doi: 10.1016/j.gep.2015.05.003. Epub 2015 Jul 2.

研究斑马鱼中生殖细胞特化的母体调控的方法。

Methods to study maternal regulation of germ cell specification in zebrafish.

作者信息

Kaufman O H, Marlow F L

机构信息

Albert Einstein College of Medicine, Bronx, NY, United States.

出版信息

Methods Cell Biol. 2016;134:1-32. doi: 10.1016/bs.mcb.2016.02.001. Epub 2016 Mar 2.

DOI:10.1016/bs.mcb.2016.02.001
PMID:27312489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5039941/
Abstract

The process by which the germ line is specified in the zebrafish embryo is under the control of maternal gene products that were produced during oogenesis. Zebrafish are highly amenable to microscopic observation of the processes governing maternal germ cell specification because early embryos are transparent, and the germ line is specified rapidly (within 4-5h post fertilization). Advantages of zebrafish over other models used to study vertebrate germ cell formation include their genetic tractability, the large numbers of progeny, and the easily manipulable genome, all of which make zebrafish an ideal system for studying the genetic regulators and cellular basis of germ cell formation and maintenance. Classical molecular biology techniques, including expression analysis through in situ hybridization and forward genetic screens, have laid the foundation for our understanding of germ cell development in zebrafish. In this chapter, we discuss some of these classic techniques, as well as recent cutting-edge methodologies that have improved our ability to visualize the process of germ cell specification and differentiation, and the tracking of specific molecules involved in these processes. Additionally, we discuss traditional and novel technologies for manipulating the zebrafish genome to identify new components through loss-of-function studies of putative germ cell regulators. Together with the numerous aforementioned advantages of zebrafish as a genetic model for studying development, we believe these new techniques will continue to advance zebrafish to the forefront for investigation of the molecular regulators of germ cell specification and germ line biology.

摘要

斑马鱼胚胎中生殖系的特化过程受卵子发生过程中产生的母源基因产物的控制。斑马鱼非常适合对母源生殖细胞特化过程进行显微镜观察,因为早期胚胎是透明的,并且生殖系特化迅速(受精后4 - 5小时内)。与用于研究脊椎动物生殖细胞形成的其他模型相比,斑马鱼的优势包括其遗传易操作性、大量的后代以及易于操作的基因组,所有这些都使斑马鱼成为研究生殖细胞形成和维持的遗传调节因子及细胞基础的理想系统。经典分子生物学技术,包括通过原位杂交进行表达分析和正向遗传筛选,为我们理解斑马鱼生殖细胞发育奠定了基础。在本章中,我们将讨论其中一些经典技术,以及最近的前沿方法,这些方法提高了我们可视化生殖细胞特化和分化过程以及追踪这些过程中涉及的特定分子的能力。此外,我们还将讨论用于操纵斑马鱼基因组以通过对假定的生殖细胞调节因子进行功能丧失研究来鉴定新成分的传统和新技术。结合斑马鱼作为研究发育的遗传模型的众多上述优势,我们相信这些新技术将继续推动斑马鱼成为研究生殖细胞特化分子调节因子和生殖系生物学的前沿。