Sharma Mukesh K, Denovan-Wright Eileen M, Degrave Agnes, Thisse Christine, Thisse Bernard, Wright Jonathan M
Department of Biology, Dalhousie University, 1355 Oxford Street, Halifax, NS, Canada B3H 4J1.
Comp Biochem Physiol B Biochem Mol Biol. 2004 Aug;138(4):391-8. doi: 10.1016/j.cbpc.2004.05.009.
The intestinal fatty acid-binding protein (I-FABP) shows binding specificity for long-chain fatty acids and is proposed to be involved in uptake of dietary fatty acids and their intracellular transport. We have determined the sequence of the gene encoding I-FABP in zebrafish. The zebrafish I-FABP gene contains four exons interrupted by three introns. Radiation hybrid mapping assigned the I-FABP gene to linkage group 1. A 924 bp sequence 5' upstream of the initiation codon in the I-FABP gene contained several putative cis-acting regulatory elements. In adult zebrafish, reverse transcription-polymerase chain reaction (RT-PCR) detected I-FABP mRNA in intestine, brain, liver, muscle and testis. Quantitative RT-PCR demonstrated that I-FABP mRNA was most abundant in intestine, followed by brain. I-FABP mRNA levels were very low in muscle, testis, heart, liver, skin and ovary. RT-PCR using total RNA extracted from zebrafish embryos detected I-FABP mRNA as early as 12 h post-fertilization. Whole-mount in situ hybridization to zebrafish embryos detected I-FABP mRNA in the yolk syncytial layer (YSL) at early somitogenesis. Later during embryonic development the I-FABP mRNA was detected in the intestinal bulb, liver and pancreas primordium. Expression in YSL, liver or pancreas has not been previously reported for fish or mammalian I-FABP genes and may be related to specific physiological differences between fishes and mammals.
肠脂肪酸结合蛋白(I-FABP)对长链脂肪酸具有结合特异性,据推测其参与膳食脂肪酸的摄取及其细胞内转运。我们已经确定了斑马鱼中编码I-FABP的基因序列。斑马鱼I-FABP基因包含四个外显子,被三个内含子隔开。辐射杂种图谱将I-FABP基因定位到连锁群1。I-FABP基因起始密码子上游5'的一段924 bp序列包含几个推定的顺式作用调控元件。在成年斑马鱼中,逆转录-聚合酶链反应(RT-PCR)在肠、脑、肝、肌肉和睾丸中检测到I-FABP mRNA。定量RT-PCR表明,I-FABP mRNA在肠中最丰富,其次是脑。I-FABP mRNA水平在肌肉、睾丸、心脏、肝脏、皮肤和卵巢中非常低。使用从斑马鱼胚胎中提取的总RNA进行RT-PCR,早在受精后12小时就检测到了I-FABP mRNA。对斑马鱼胚胎进行的全胚胎原位杂交在早期体节形成时在卵黄合胞体层(YSL)中检测到I-FABP mRNA。在胚胎发育后期,在肠球、肝脏和胰腺原基中检测到I-FABP mRNA。鱼类或哺乳动物的I-FABP基因以前尚未报道过在YSL、肝脏或胰腺中的表达,这可能与鱼类和哺乳动物之间特定的生理差异有关。