Trieu V N, Hasler-Rapacz J, Rapacz J, Black D D
Department of Pediatrics, University of Chicago, Pritzker School of Medicine, IL 60637.
Gene. 1993 Jan 30;123(2):173-9. doi: 10.1016/0378-1119(93)90121-i.
Apolipoprotein A-I (ApoA-I) is the principal protein component of plasma high-density lipoprotein (HDL) and an activator of lecithin:cholesterol acyltransferase. Apolipoprotein C-III (ApoC-III) exchanges between triglyceride-rich lipoproteins and HDL and inhibits the lipolysis and uptake of triglyceride-rich lipoproteins. To study the expression of these Apo-encoding genes in the developing swine, apoA-I and apoC-III cDNAs from a lambda gt11 porcine liver cDNA library and apoC-III from a porcine genomic DNA library were isolated and sequenced. The predicted amino acid (aa) sequence and composition for ApoC-III matched the N-terminal aa sequence and composition of purified swine ApoC-III. Comparison among known ApoA-I and C-III aa sequences from various species revealed strict conservation of amphipathic helices. In adult pigs, the apoA-I mRNA was found predominantly in the intestine and liver, with a small amount detected in the testes. In contrast, apoC-III mRNA was found predominantly in adult liver. Developmentally, hepatic apoA-I and apoC-III mRNAs were expressed in livers of fetal, newborn, and suckling animals. Intestinal apoA-I and apoC-III mRNAs, however, were detected only in postpartum animals. Although intestinal apoA-I mRNA expression continued into the adult, intestinal apoC-III mRNA expression declined sharply after the newborn period.
载脂蛋白A-I(ApoA-I)是血浆高密度脂蛋白(HDL)的主要蛋白质成分,也是卵磷脂胆固醇酰基转移酶的激活剂。载脂蛋白C-III(ApoC-III)在富含甘油三酯的脂蛋白和HDL之间交换,并抑制富含甘油三酯的脂蛋白的脂解和摄取。为了研究这些载脂蛋白编码基因在发育中的猪体内的表达情况,从λgt11猪肝脏cDNA文库中分离并测序了apoA-I和apoC-III cDNA,以及从猪基因组DNA文库中分离并测序了apoC-III。预测的ApoC-III氨基酸(aa)序列和组成与纯化的猪ApoC-III的N端aa序列和组成相匹配。对来自不同物种的已知ApoA-I和C-III aa序列进行比较,发现两亲性螺旋严格保守。在成年猪中,apoA-I mRNA主要在肠道和肝脏中发现,在睾丸中检测到少量。相比之下,apoC-III mRNA主要在成年肝脏中发现。在发育过程中,肝脏中的apoA-I和apoC-III mRNA在胎儿、新生儿和哺乳期动物的肝脏中表达。然而,肠道中的apoA-I和apoC-III mRNA仅在产后动物中检测到。尽管肠道apoA-I mRNA表达持续到成年,但肠道apoC-III mRNA表达在新生儿期后急剧下降。