Isolation of Differentially Expressed Transcripts by cDNA-AFLPaba and Expression Analysis of DEAD Box ATP-Dependent RNA Helicase 48 in Ovaries of the Giant Tiger Shrimp Penaeus monodon

Q4 Agricultural and Biological Sciences Genetics of Aquatic Organisms Pub Date : 2020-09-25 DOI:10.4194/2459-1831-V4_2_04
S. Klinbunga, Sirikan Prasertlux, Sirithorn Janpoom, Puttawan Romgmung, B. Khamnamtong
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引用次数: 1

Abstract

Genes involved in ovarian development of the giant tiger shrimp (Penaeus monodon) were isolated by cDNA-AFLP analysis. In total, 75 primer combinations were screened against cDNA of different stages of ovaries (premature ovaries of juveniles and previtellogenic, vitellogenic and mature ovaries of wild intact and eyestalk-ablated broodstock; N = 6 for each group). Eighteen cDNA-AFLP fragments were cloned and sequenced. Nucleotide sequences of ten fragments significantly matched EF-1α (7e63), DEAD box ATP-dependent RNA helicase 48 (PmDdx48; 8e-61), tyrosine phosphatase n9 (1e-42), autophagy related protein Atg4-like protein (3e-36), nuclear pore complex protein nup154 (6e-20), GK14382 gene product (1e-20), L-3-hydroxyacryl coenzyme A dehydrogenase short chain (8e-13) and three different hypothetical proteins. The remaining fragments did not match any previously deposited sequence (E-value > 10-4). The full-length cDNA of PmDdx48 was successfully characterized. It was 1646 bp containing an open reading frame (ORF) of 1209 bp corresponding to 402 amino acids. PmDdx48 was up-regulated in late vitellogenic and mature ovaries of wild intact broodstock and in mature ovaries of wild eyestalk-ablated broodstock (P<0.05). Unilateral eyestalk ablation resulted in down-regulation of PmDdx48 in late vitellogenic and mature ovaries compared to that of wild intact broodstock (P<0.05).
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cdna - aflaba分离差异表达转录物及DEAD Box atp依赖性RNA解旋酶48在单对虾卵巢中的表达分析
采用cDNA AFLP分析方法,分离出了参与斑节对虾卵巢发育的基因。总共筛选了75个引物组合,以对抗不同阶段卵巢的cDNA(幼鱼的过早卵巢和野生完整和去除眼柄的亲代的前胚胎、卵黄和成熟卵巢;每组N=6)。克隆并测序了18个cDNA AFLP片段。10个片段的核苷酸序列与EF-1α(7e63)、DEAD-box-ATP依赖性RNA解旋酶48(PmDdx48;8e-61)、酪氨酸磷酸酶n9(1e-42)、自噬相关蛋白Atg4样蛋白(3e-36)、核孔复合体蛋白nup154(6e-20)、GK14382基因产物(1e-20),L-3-羟基丙烯酰辅酶A脱氢酶短链(8e-13)和三种不同的假设蛋白显著匹配。剩余的片段与之前沉积的任何序列都不匹配(E值>10-4)。成功鉴定了PmDdx48的全长cDNA。其长度为1646bp,包含1209bp的开放阅读框(ORF),对应402个氨基酸。PmDdx48在野生完整亲鱼的晚卵黄和成熟卵巢以及切除野生眼柄的亲鱼的成熟卵巢中上调(P<0.05)。
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来源期刊
Genetics of Aquatic Organisms
Genetics of Aquatic Organisms Agricultural and Biological Sciences-Aquatic Science
CiteScore
0.90
自引率
0.00%
发文量
8
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