2003
DOI: 10.1023/b:fish.0000045723.52428.5e
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Primary structures and gene organizations of two types of Wap65 from the pufferfish Takifugu rubripes

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Cited by 30 publications
(39 citation statements)
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“…Further analyses on other fish species (Oncorhynchus mykiss, Ictalurus punctatus, Danio rerio, Oryzias latipes and Takifugu rubripes) have shown that in contrast to the single isoform found in mammals, wap65 is present in duplicate in fish, presumably as a result of the teleost whole genome duplication event (Amores et al, 1998). These fish isoforms display different affinities for haem, tissue distributions and development patterns (Hirayama et al, 2003;2004;Nakaniwa et al, 2005). In contrast to the eurythermal examples quoted earlier, some animals exist within a very narrow environmental temperature envelope.…”
Section: Introductionmentioning
confidence: 81%
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“…Further analyses on other fish species (Oncorhynchus mykiss, Ictalurus punctatus, Danio rerio, Oryzias latipes and Takifugu rubripes) have shown that in contrast to the single isoform found in mammals, wap65 is present in duplicate in fish, presumably as a result of the teleost whole genome duplication event (Amores et al, 1998). These fish isoforms display different affinities for haem, tissue distributions and development patterns (Hirayama et al, 2003;2004;Nakaniwa et al, 2005). In contrast to the eurythermal examples quoted earlier, some animals exist within a very narrow environmental temperature envelope.…”
Section: Introductionmentioning
confidence: 81%
“…Wap65-2 has a much more restricted tissue distribution (mainly liver), compared to wap65-1, which is present in multiple tissues in O. latipes and Takifugu (Hirayama et al, 2003;2004). In spite of the presence of the two conserved histidine residues proposed to be essential for haem binding, other fish orthologues of Wap65-2, which also contain these residues, do not show an affinity for haem (Hirayama et al, 2004).…”
Section: Discussionmentioning
confidence: 99%
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“…Wap65 was first detected as a glycoprotein in the plasma of goldfish (Kikuchi et al 1993) and has since been identified in medaka (Oryzias latipes), channel catfish (Ictalurus punctatus), swordtail fish (Xiphophorus hellerii), and fugu (Takifigu rubripes) (Kikuchi et al 1995;Kinoshita et al 2001;Hirayama et al 2003Hirayama et al , 2004Nakaniwa et al 2005;Aliza et al 2008). Teleost Wap65 shares significant sequence identity with mammalian hemopexin and has been suggested to play roles in iron homeostasis, antioxidant activity, bacteriostatic defense, nerve regeneration, transfer of heme, and the expression of genes known to promote cell survival (Delanghe and Langlois 2001).…”
Section: Introductionmentioning
confidence: 99%
“…因其与暖温适应相关且相对分子质量为 6.5×10 4 而 得名。 该类蛋白存在 Wap65-1 和 Wap65-2 两种异构 体 (Hirayama et al, 2003)。研究表明, Wap65-2 具有 多种生物学功能, 它与鱼类暖温适应 (Hirayama et al, 2003)、重金属胁迫 (Aliza et al, 2008)和生长发育 (Hirayama et al, 2004) 等 紧 密 相 关 。 近 年 来 , Wap65-2 在细菌感染性免疫应激中的作用日益引起 人们的关注 (Cho et al, 2012;Li et al, 2011;Peatman et al, 2008;Sha et al, 2008;Shi et al, 2010)。目前, 多种鱼类 Wap65-2 基因序列已被克隆, 包括东方红 鳍鲀(Takifugu rubripes) (Hirayama et al, 2003)、青鳉 (Oryzias latipes) (Hirayama et al, 2004) 、 蓝 鲇 (Ictalurus furcatus) (Peatman et al, 2008)、斑点叉尾 鮰 (I. punctatus) (Sha et al, 2008) 、 剑 尾 鱼 (Xiphophorus hellerii) (Aliza et al, 2008)、真裸南极 鱼(Harpagifer antarcticus) (Clak & Burns, 2008)、香 鱼(Plecoglossus altivelis) (Shi et al, 2010)、欧洲海鲈 (Dicentrarchus labrax) (Sarropoulou et al, 2010)和大 鳞泥鳅(Misgurnus mizolepis) (Cho et al, 2012 (Li et al, 2009)…”
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