Ponce Marian, Infante Carlos, Funes Victoria, Manchado Manuel
IFAPA Centro El Toruño, Camino Tiro de Pichón s/n, 11500 El Puerto de Santa María (Cádiz), Spain.
Comp Biochem Physiol B Biochem Mol Biol. 2008 Aug;150(4):418-26. doi: 10.1016/j.cbpb.2008.04.013. Epub 2008 May 1.
Insulin-like growth factors (IGFs) I and II (IGF-I and IGF-II) play important roles in fish growth and development. The present study was aimed at isolating cDNAs encoding both IGF-I and IGF-II in the redbanded seabream (Pagrus auriga), and at measuring relative gene expression levels in different organs and during larval development. A fragment of 1321 nucleotides coding for IGF-I was cloned from liver using 3' and 5' RACE techniques. It included an open reading frame of 558 nucleotides, encoding a 185-amino acid preproIGF-I. With respect to IGF-II, a fragment of 1544 nucleotides was cloned as well. The open reading frame spanned 648 nucleotides, rendering a 215-amino acid preproIGF-II. The deduced mature 67-amino acid IGF-I and 70-amino acid IGF-II exhibited high sequence identities with their corresponding fish counterparts, ranging between 88.6-100% and 79.1-98.5%, respectively. Real-time PCR showed the highest IGF-I transcripts in liver ( approximately 200-fold higher than head-kidney). In contrast, the highest IGF-II mRNAs were detected in gills and heart ( approximately 16-fold higher than head-kidney). In addition, both IGFs exhibited different gene expression patterns during larval development suggesting that their expression is developmentally regulated. IGF-I reached the highest expression levels at 18 days after hatching (11.6-fold higher than 1 day after hatching), whereas IGF-II expression did not change significantly. Both hepatic IGF-I and IGF-II mRNA levels increased sharply (3.1- and 19-fold higher than control, respectively) 3 h after injection of porcine growth hormone, but remained unchanged from 6 to 24 h after treatment. Our results are discussed in relation to those previously reported for other bony fish.
胰岛素样生长因子(IGFs)I和II(IGF-I和IGF-II)在鱼类生长和发育中发挥着重要作用。本研究旨在分离编码红鳍笛鲷(Pagrus auriga)IGF-I和IGF-II的cDNA,并测定不同器官以及幼体发育过程中的相对基因表达水平。利用3'和5' RACE技术从肝脏中克隆出一段1321个核苷酸的编码IGF-I的片段。它包含一个558个核苷酸的开放阅读框,编码一个185个氨基酸的前胰岛素原IGF-I。关于IGF-II,也克隆出了一段1544个核苷酸的片段。开放阅读框跨度为648个核苷酸,产生一个215个氨基酸的前胰岛素原IGF-II。推导的成熟的67个氨基酸的IGF-I和70个氨基酸的IGF-II与其相应的鱼类对应物具有高度的序列同一性,分别在88.6 - 100%和79.1 - 98.5%之间。实时PCR显示肝脏中IGF-I转录本最高(比头肾高约200倍)。相比之下,鳃和心脏中检测到的IGF-II mRNA最高(比头肾高约16倍)。此外,两种IGF在幼体发育过程中表现出不同的基因表达模式,表明它们的表达受发育调控。IGF-I在孵化后18天达到最高表达水平(比孵化后1天高11.6倍),而IGF-II表达没有显著变化。注射猪生长激素3小时后,肝脏中IGF-I和IGF-II的mRNA水平均急剧增加(分别比对照高3.1倍和19倍),但在处理后6至24小时保持不变。我们将我们的结果与先前报道的其他硬骨鱼的结果进行了讨论。