Abbott B D, Probst M R
Developmental Toxicology Division, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.
Dev Dyn. 1995 Oct;204(2):144-55. doi: 10.1002/aja.1002040205.
The aryl hydrocarbon receptor (AhR) and the AhR nuclear translocator protein (ARNT) are basic-helix-loop-helix (bHLH) proteins involved in transcriptional regulation. The AhR is a ligand-activated partner of the ARNT protein. Both proteins are required to transcriptionally regulate gene expression. ARNT must be complexed to AhR to permit binding to the regulatory DNA sequence. The AhR-ligand complex is known to mediate a range of biological responses, such as developmental toxicity, induction of cleft palate, and hydronephrosis. AhR and ARNT are expressed in human embryonic palatal cells and AhR was recently shown to have a specific developmental pattern of expression in the mouse embryo. In the present study, expression of ARNT is characterized in C57Bl/6N mouse embryos from gestation day (GD) 10-16 using immunohistochemistry and in situ hybridization. Af affinity purified antibody against human ARNT (1.1 micrograms/ml) was detected with an avidin-biotin-peroxidase complex. ARNT mRNA was localized with a 35S-RNA probe from pBM5/NEO-M1-1. Specific spatial and temporal patterns of ARNT expression emerged and mRNA and protein expression correlated. The GD 10-11 embryos showed highest levels of ARNT in neuroepithelial cells of the neural tube, visceral arches, otic and optic placodes, and preganglionic complexes. The heart also had significant expression of ARNT with strong nuclear localization. After GD11, expression in heart and brain declined. In GD 12-13 embryos expression was highest in the liver where expression increased from GD 12-16. At GD 15-16 the highest levels of ARNT occurred in adrenal gland and liver, although ARNT was also detected in submandibular gland, ectoderm, tongue, bone, and muscle. In all of these tissues ARNT was cytoplasmic as well as nuclear, except in some of the cortical adrenal cells in which ARNT was strongly cytoplasmic with little or no nuclear localization. These specific patterns of ARNT expression, which differ in certain tissues from the expression of AhR, suggest that ARNT may have additional roles in normal embryonic development.
芳基烃受体(AhR)和AhR核转运蛋白(ARNT)是参与转录调控的碱性螺旋-环-螺旋(bHLH)蛋白。AhR是ARNT蛋白的配体激活伴侣。两种蛋白都是转录调控基因表达所必需的。ARNT必须与AhR形成复合物才能与调控DNA序列结合。已知AhR-配体复合物可介导一系列生物学反应,如发育毒性、腭裂诱导和肾积水。AhR和ARNT在人胚胎腭细胞中表达,最近发现AhR在小鼠胚胎中有特定的发育表达模式。在本研究中,使用免疫组织化学和原位杂交技术对妊娠第10 - 16天的C57Bl/6N小鼠胚胎中ARNT的表达进行了表征。用抗人ARNT的亲和纯化抗体(1.1微克/毫升)与抗生物素蛋白-生物素-过氧化物酶复合物进行检测。用来自pBM5/NEO-M1-1的35S-RNA探针定位ARNT mRNA。出现了ARNT表达的特定时空模式,且mRNA和蛋白表达相关。妊娠第10 - 11天的胚胎在神经管的神经上皮细胞、内脏弓、耳和视板以及神经节前复合物中显示出最高水平的ARNT。心脏也有显著的ARNT表达,且有强烈的核定位。妊娠第11天后,心脏和大脑中的表达下降。在妊娠第12 - 13天的胚胎中,肝脏中的表达最高,从妊娠第12天到第16天表达增加。在妊娠第15 - 16天,肾上腺和肝脏中ARNT水平最高,尽管在下颌下腺、外胚层、舌头、骨骼和肌肉中也检测到了ARNT。在所有这些组织中,ARNT既有细胞质表达也有核表达,但在一些皮质肾上腺细胞中,ARNT主要是细胞质表达,几乎没有或没有核定位。ARNT这些特定的表达模式在某些组织中与AhR的表达不同,这表明ARNT在正常胚胎发育中可能具有额外的作用。