scispace - formally typeset
Open AccessJournal ArticleDOI

Developmental expression of two members of a new class of transcription factors: I. Expression of aryl hydrocarbon receptor in the C57BL/6N mouse embryo

Reads0
Chats0
TLDR
Examination of the pattern of AhR expression in the C57BL/6N mouse embryo from gestation days (GD) 10–16 suggests that this novel ligand‐activated transcriptional regulator may be important in normal embryonic development.
Abstract
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor with a basic region/helix-loop-helix (bHLH) motif. AhR has been sequenced and the functional domains defined and there is information on the formation of complexes with other peptides and interactions with DNA, although these areas continue to be investigated. AhR mediates many biological effects such as developmental toxicity, including induction of cleft palate and hydronephrosis. This regulatory protein is expressed in embryonic liver and has been immunohistochemically localized in cells of human and mouse secondary palate. The expression of AhR in embryonic tissues and its ability to disrupt development suggests a significant role for this protein in development. The present study examines the pattern of AhR expression in the C57BL/6N mouse embryo from gestation days (GD) 10–16, using in situ hybridization and immunohistochemical analysis. AhR mRNA was localized with 35S-RNA antisense riboprobe (cAh1 probe, 1.8 Kb amino terminal DNA). AhR protein was localized with purified monoclonal antibody (RPT-9) raised against the N-terminal peptide sequence. AhR mRNA and protein were expressed in GD 10–13 neuroepithelium, and as development progressed the levels in brain decreased. GD 10–12 embryos also showed AhR in branchial arches, heart, somites, and liver. AhR protein and mRNA in heart were highest at GD 10–11 and decreased with age. In liver, AhR mRNA and protein levels increased and nuclear localization became more pronounced with gestational age. In GD 14–16 embryos levels in liver and adrenal were highest, but AhR was present in ectoderm, bone, and muscle. AhR expression was specific for both cell type, organ/tissue, and developmental stage, suggesting that this novel ligand-activated transcriptional regulator may be important in normal embryonic development. © 1995 wiley-Liss, Inc.1

read more

Citations
More filters
Journal ArticleDOI

Ah receptor signaling pathways

TL;DR: The objective is to review the Ah receptor's role in regulation of xenobiotic metabolism and use this model as a framework for understanding the less well-characterized mechanism of dioxin toxicity.
Journal ArticleDOI

Loss of teratogenic response to 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD) in mice lacking the Ah (dioxin) receptor

TL;DR: There is no direct proof that the AhR is involved in the teratogenic effects of TCDD, but the role of AhR in the regulatory mechanism of xenobiotic‐metabolizing enzymes is investigated.
Journal ArticleDOI

Cancer and developmental exposure to endocrine disruptors.

TL;DR: Findings suggest that causes of endocrine-related cancers or susceptibility to cancer may be a result of developmental exposures rather than exposures existing at or near the time of tumor detection.
Journal ArticleDOI

The aryl hydrocarbon receptor cross-talks with multiple signal transduction pathways.

TL;DR: The effect of a particular AHR ligand may depend as much on the adaptive interactions that it established with pathways and proteins expressed in a specific cell or tissue as on the toxic responses that it raises.
Journal ArticleDOI

The aryl hydrocarbon receptor: A comparative perspective

TL;DR: In this review, the current understanding of the AHR signal transduction pathway in non-mammalian and other non-traditional species is summarized, with an emphasis on similarities and differences in comparison to the A HR pathway in rodents and humans.
References
More filters
Journal ArticleDOI

2,3,7,8-Tetrachlorodibenzo-p-Dioxin and Related Halogenated Aromatic Hydrocarbons: Examination of the Mechanism of Toxicity

TL;DR: The toxicity of halogenated aromatic hydrocarbons appears to be due to the sustained expression of a normal cellular regulatory system, of which the author was previously unaware.
Journal ArticleDOI

Cloning of a factor required for activity of the Ah (dioxin) receptor.

TL;DR: The complementary DNA and part of the gene for an 87-kilodalton human protein that is necessary for Ah receptor function have been cloned and two portions of the protein share sequence similarities with two Drosophila proteins, Per and Sim.
Journal ArticleDOI

Cloning of the Ah-receptor cDNA reveals a distinctive ligand-activated transcription factor.

TL;DR: A cDNA encoding the murine Ah receptor (Ahb-1 allele for aromatic hydrocarbon responsiveness) has been isolated and characterized in this article, which revealed a region with similarity to the basic region/helix-loop-helix (BR/HLH) motif found in many transcription factors that undergo dimerization for function.
Journal ArticleDOI

Identification of the Ah receptor nuclear translocator protein (Arnt) as a component of the DNA binding form of the Ah receptor.

TL;DR: Arnt is now shown to be a structural component of the XRE binding form of the Ah receptor, and and the ligand-binding subunit of the receptor were extracted as a complex from the nuclei of cells treated with ligand.
Journal ArticleDOI

Developmental and Reproductive Toxicity of Dioxins and Related Compounds: Cross-Species Comparisons

TL;DR: Decreases in spermatogenesis and the ability to conceive and carry a pregnancy to term are the most sensitive signs of reproductive toxicity in male and female mammals, respectively.
Related Papers (5)