NKX-2.5 - A NOVEL MURINE HOMEOBOX GENE EXPRESSED IN EARLY HEART PROGENITOR CELLS AND THEIR MYOGENIC DESCENDANTS
- Author(s)
- Lints, TJ; Parsons, LM; Hartley, L; Lyons, I; Harvey, RP;
- Details
- Publication Year 1993-10,Volume 119,Issue #2,Page 419-431
- Journal Title
- DEVELOPMENT
- Publication Type
- Journal Article
- Abstract
- We have isolated two murine homeobox genes, Nkx-2.5 and Nkx-2.6, that are new members of a sp sub-family of homeobox genes related to Drosophila NK2, NK3 and NK4/msh-2. In this paper, we focus on the Nkx-2.5 gene and its expression pattern during post-implantation development. Nkx-2.5 transcripts are first detected at early headfold stages in myocardiogenic progenitor cells. Expression preceeds the onset of myogenic differentiation, and continues in cardiomyocytes of embryonic, foetal and adult hearts. Transcripts are also detected in future pharyngeal endoderm, the tissue believed to produce the heart inducer. Expression in endoderm is only found laterally, where it is in direct apposition to promyocardium, suggesting an interaction between the two tissues. After foregut closure, Nkx-2.5 expression in endoderm is limited to the pharyngeal floor, dorsal to the developing heart tube. The thyroid primordium, a derivative of the pharyngeal floor, continues to express Nkx-2.5 after transcript levels diminish in the rest of the pharynx. Nkx-2.5 transcripts are also detected in lingual muscle, spleen and stomach. The expression data implicate Nkx-2.5 in commitment to and/or differentiation of the myocardial lineage. The data further demonstrate that cardiogenic progenitors can be distinguished at a molecular level by late gastrulation. Nkx-2.5 expression will therefore be a valuable marker in the analysis of mesoderm development and an early entry point for dissection of the molecular basis of myogenesis in the heart.
- Publisher
- COMPANY OF BIOLOGISTS LTD
- Keywords
- DROSOPHILA EMBRYOS; TRANSCRIPTION FACTOR; TRANSGENIC MICE; GROWTH-FACTORS; MOUSE EMBRYOS; HOMEODOMAIN; MUSCLE; LINES; DIFFERENTIATION; SPECIFICITY
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Creation Date: 1993-10-01 12:00:00