Sequence analysis, chromosomal location, and developmental expression of the mouse preproendothelin-1 gene

K Maemura, H Kurihara, Y Kurihara, H Oda, T Ishikawa… - Genomics, 1996 - Elsevier
K Maemura, H Kurihara, Y Kurihara, H Oda, T Ishikawa, NG Copeland, DJ Gilbert…
Genomics, 1996Elsevier
Recent studies have designated endothelins (ETs) as morphogenetic factors in embryonic
development. In the present study, we cloned and characterized the mouse
preproendothelin-1 (preproET-1) gene (Edn1) and examined its expression in reference to
development. Edn1comprises five exons, and the open reading frame encodes the 202-
amino-acid preproET-1. The sequences and structural organization ofEdn1are highly
homologous to those of other species, especially in the terminal 200-bp sequence of the 3 …
Recent studies have designated endothelins (ETs) as morphogenetic factors in embryonic development. In the present study, we cloned and characterized the mouse preproendothelin-1 (preproET-1) gene (Edn1) and examined its expression in reference to development.Edn1comprises five exons, and the open reading frame encodes the 202-amino-acid preproET-1. The sequences and structural organization ofEdn1are highly homologous to those of other species, especially in the terminal 200-bp sequence of the 3′-noncoding region. Interspecific backcross mapping locatedEdn1in the central region of chromosomal 13, where a mouse mutation, congenital hydrocephalus (ch), is also mapped. The highest expression ofEdn1mRNA is detected in the lung in adult mice, whereasEdn1is predominantly expressed in the epithelium and mesenchyme of the pharyngeal arches and in the endothelium of the large arteries.Edn1expression and ET-1 peptide levels in the lung progressively increase during the perinatal stage, whereas the expression ofEdn3,a gene encoding ET-3, reciprocally decreases. These results suggest thatEdn1expression is developmentally regulated in different tissues and organs in mice in a spatial- and temporal-specific manner.
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