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首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Nanos3 not nanos1 and nanos2 is a germ cell marker gene in large yellow croaker during embryogenesis
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Nanos3 not nanos1 and nanos2 is a germ cell marker gene in large yellow croaker during embryogenesis

机译:NaNOS3不是纳米1和纳米2是胚胎发生期间大黄叉胶中的生殖细胞标志物基因

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摘要

In this study, three nanos gene subtypes (Lcnanosl, Lcnanos2 and Lcnanos3) from Larimichthys crocea, were cloned and characterized. We determined the spatio-temporal expression patterns of each subtype in tissues as well as the cellular localization of mRNA in embryos. Results showed that deduced Nanos proteins have two main homology domains: N-terminal CCR4/NOT1 deadenylase interaction domain and highly conserved car boxy-terminal region bearing two conserved CCHC zinc-finger motifs. The expression levels of Lcnanosl in testis were significantly higher than other tissues, followed by heart, brain, eye, and ovary. Nevertheless, both Lcnanos2 and Lcnanos3 were restrictedly expressed in testis and ovary, respectively. No signals of Lcnanosl and Lcnanos2 expression were detected at any developmental stages during embryogenesis. On the contrary, the signals of Lcnanos3 were detected in all stages examined. Lcnanos3 transcripts were firstly localized to the distal end of cleavage furrow at the 2-cell stage. Subsequently, mounting positive signals started to appear in a small number of cells as the embryo developed to blastula stage and early-gastrula stage. As development proceeded, positive signals were found in the primitive gonadal ridge. These cells of Lcnanos3 positive signals implied the specification of the future PGCs at this stage. It also suggested that PGCs of croaker originate from four clusters of cells which inherit maternal germ plasm at blastula stage. Furthermore, we preliminarily analyzed the migration route of PGCs in embryos of L. crocea. In short, this study laid the foundation for studies on specification and development of germ cell from L. crocea during embryogenesis.
机译:在该研究中,克隆并表征了来自Larimichthys Crocea的三种纳米基因亚型(LcnAnosl,LcnAnos2和Lcnanos3)。我们确定组织中每种亚型的时空表达模式以及胚胎中mRNA的细胞定位。结果表明,推导的纳米蛋白具有两个主要同源域:N-末端CCR4 / NOT1硬苯基酶相互作用域和高度保守的汽车箱末端区域轴承两个保守的CCHC锌手指基序。睾丸中LcnAnosl的表达水平明显高于其他组织,然后是心脏,脑,眼睛和卵巢。然而,LCNANOS2和LCNANOS3分别在睾丸和卵巢中被限制在睾丸和卵巢中。在胚胎发生期间,在任何发育阶段中检测到LCNANOS1和LCNANOS2表达的信号。相反,在检查的所有阶段中检测到LCNANOS3的信号。将LCNANOS3转录物首先定位在2细胞阶段的切割沟槽的远端。随后,安装正信号在较少的细胞中开始出现在胚胎上发育到Blastula阶段和早期腹部阶段。随着开发进行的,在原始的Gonadal山脊中发现了正信号。这些LCNANOS3正信号的细胞在该阶段暗示了未来PGC的规范。它还表明Crokaker的PGCS源自四种细胞簇,其在Blastula阶段继承母体胚芽血浆。此外,我们预先分析了L. Crocea胚胎中PGCs的迁移路径。简而言之,本研究为胚胎发生期间L. Crocea的种质和发育研究奠定了基础。

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