National Engineering Laboratory for Animal Breeding, College of Animal Science and Technology, China Agricultural University, Beijing 100193, China.
Poult Sci. 2012 Sep;91(9):2275-81. doi: 10.3382/ps.2012-02197.
Nitric oxide (NO), an endothelium-derived relaxing factor, is synthesized from l-arginine by endothelial nitric oxide synthase (eNOS) in the endothelium. The objective of the present study was to preliminarily illuminate the expression of the eNOS gene in hypoxic adaptation of chicken embryonic development. The eNOS expression profiles between the Tibet and Shouguang chickens incubated under both normoxic and hypoxic conditions were detected by TaqMan real-time PCR. In this study, the chicken eNOS gene was found by both in silico cloning and RACE approaches. From the eNOS gene, we obtained a 3,310-bp mRNA sequence and a 10,666-bp DNA sequence and discovered that it was located on chicken chromosome 2 and had 7 unique transcripts. eNOS mRNA was detected in abundant amounts in some chick embryo organs (i.e., heart, liver, chorio-allantoic membrane, and lung), and expressed stably with the lowest levels in the brain. We observed that when exposed to hypoxia (13% O(2)) different embryo organ tissues had various sensitivities to hypoxia as determined by their eNOS expression profiles. Compared with the Shouguang chicken, the eNOS expression in the Tibet chicken was higher in the lung and liver, lower in the heart, and similar in the brain. In chorio-allantoic membranes, eNOS expression was higher in the Shouguang chicken than the Tibet chicken under hypoxic conditions, but not markedly different under normoxic conditions. The differences of eNOS expression between the 2 breeds may be relative to the hypoxic adaptation ability in Tibet chickens during embryonic development. This work will provide reference for future studies on the role of eNOS in hypoxic adaptation and response.
一氧化氮(NO)是一种内皮衍生的舒张因子,由内皮细胞中的内皮型一氧化氮合酶(eNOS)从 l-精氨酸合成。本研究的目的是初步阐明 eNOS 基因在鸡胚胎发育缺氧适应中的表达。通过 TaqMan 实时 PCR 检测了在常氧和缺氧条件下培养的藏鸡和寿光鸡中 eNOS 基因的表达谱。在本研究中,通过计算机克隆和 RACE 方法发现了鸡 eNOS 基因。从 eNOS 基因中,我们获得了一个 3310bp 的 mRNA 序列和一个 10666bp 的 DNA 序列,并发现它位于鸡染色体 2 上,有 7 个独特的转录本。eNOS mRNA 在一些鸡胚器官(即心脏、肝脏、绒毛尿囊膜和肺)中大量表达,在脑中表达水平最低且稳定。我们观察到,当暴露于缺氧(13% O2)时,不同的胚胎器官组织对缺氧的敏感性不同,这可以通过它们的 eNOS 表达谱来确定。与寿光鸡相比,藏鸡的肺和肝中 eNOS 的表达较高,心脏中表达较低,脑中表达相似。在绒毛尿囊膜中,缺氧条件下寿光鸡的 eNOS 表达高于藏鸡,但在常氧条件下差异不显著。这两个品种之间 eNOS 表达的差异可能与藏鸡在胚胎发育过程中的缺氧适应能力有关。这项工作将为未来研究 eNOS 在缺氧适应和反应中的作用提供参考。