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鉴定和迁移大西洋鲑鱼的原始生殖细胞:vasa、dead end 和淋巴细胞抗原 75 基因的特征。

Identification and migration of primordial germ cells in Atlantic salmon, Salmo salar: characterization of vasa, dead end, and lymphocyte antigen 75 genes.

机构信息

Faculty of Biosciences and Aquaculture, University of Nordland, Bodø, Norway.

出版信息

Mol Reprod Dev. 2013 Feb;80(2):118-31. doi: 10.1002/mrd.22142. Epub 2013 Feb 5.

DOI:10.1002/mrd.22142
PMID:23239145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3664433/
Abstract

No information exists on the identification of primordial germ cells (PGCs) in the super-order Protacanthopterygii, which includes the Salmonidae family and Atlantic salmon (Salmo salar L.), one of the most commercially important aquatic animals worldwide. In order to identify salmon PGCs, we cloned the full-length cDNA of vasa, dead end (dnd), and lymphocyte antigen 75 (ly75/CD205) genes as germ cell marker candidates, and analyzed their expression patterns in both adult and embryonic stages of Atlantic salmon. Semi-quantitative RT-PCR results showed that salmon vasa and dnd were specifically expressed in testis and ovary, and vasa, dnd, and ly75 mRNA were maternally deposited in the egg. vasa mRNA was consistently detected throughout embryogenesis while dnd and ly75 mRNA were gradually degraded during cleavages. In situ analysis revealed the localization of vasa and dnd mRNA and Ly75 protein in PGCs of hatched larvae. Whole-mount in situ hybridization detected vasa mRNA during embryogenesis, showing a distribution pattern somewhat different to that of zebrafish; specifically, at mid-blastula stage, vasa-expressing cells were randomly distributed at the central part of blastodisc, and then they migrated to the presumptive region of embryonic shield. Therefore, the typical vasa localization pattern of four clusters during blastulation, as found in zebrafish, was not present in Atlantic salmon. In addition, salmon PGCs could be specifically labeled with a green fluorescence protein (GFP) using gfp-rt-vasa 3'-UTR RNA microinjection for further applications. These findings may assist in understanding PGC development not only in Atlantic salmon but also in other salmonids.

摘要

在包括鲑科鱼类和大西洋鲑(Salmo salar L.)在内的超纲硬骨鱼中,尚未发现原始生殖细胞(PGC)的鉴定信息。大西洋鲑是世界上最重要的商业水产动物之一。为了鉴定鲑鱼的 PGC,我们克隆了全长 cDNA 的 vasa、dead end (dnd) 和淋巴细胞抗原 75 (ly75/CD205) 基因作为候选的生殖细胞标记物,并分析了它们在大西洋鲑成鱼和胚胎发育阶段的表达模式。半定量 RT-PCR 结果表明,鲑鱼 vasa 和 dnd 特异性表达于睾丸和卵巢,vasa、dnd 和 ly75 mRNA 呈母源性沉积于卵中。vasa mRNA 在整个胚胎发生过程中持续检测到,而 dnd 和 ly75 mRNA 在卵裂过程中逐渐降解。原位分析揭示了孵化幼虫 PGC 中 vasa 和 dnd mRNA 和 Ly75 蛋白的定位。胚胎发生过程中的整体原位杂交检测到 vasa mRNA,其分布模式与斑马鱼略有不同;具体而言,在中囊胚期,vasa 表达细胞随机分布于胚盘中央部分,然后迁移到胚胎盾的假定区域。因此,在大西洋鲑中,没有发现如在斑马鱼中那样在囊胚期存在的典型的 vasa 四个簇的定位模式。此外,使用 gfp-rt-vasa 3'-UTR RNA 显微注射可以特异性标记鲑鱼 PGC,并用绿色荧光蛋白(GFP)标记,以便进一步应用。这些发现可能有助于不仅在大西洋鲑中,而且在其他鲑科鱼类中理解 PGC 发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/d46dc035dc1c/mrd0080-0118-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/50064e1ef0a2/mrd0080-0118-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/7933703cd670/mrd0080-0118-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/5276ef107f63/mrd0080-0118-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/2f3f85d17b9b/mrd0080-0118-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/d46dc035dc1c/mrd0080-0118-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/50064e1ef0a2/mrd0080-0118-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/7933703cd670/mrd0080-0118-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/5276ef107f63/mrd0080-0118-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/2f3f85d17b9b/mrd0080-0118-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554e/3664433/d46dc035dc1c/mrd0080-0118-f5.jpg

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