Abstract
The recently described NK2 family of homeodomain proteins are key developmental regulators. In Drosophila melanogaster, two members of this family, bagpipe and tinman, are required for visceral and cardiac mesoderm formation, respectively. In vertebrates, tinman appears to represent a family of closely related NK2 genes, including Nkx-2.5, that are expressed at an early stage in precardiac cells. Consistent with a role for Nkx-2.5 in heart development, inactivation of the Nkx-2.5 gene in mice causes severe cardiac malformations and embryonic lethality. However, little is known about the molecular action of Nkx-2.5 and its targets in cardiac muscle. In this paper, we report the identification and characterization of a functional and highly conserved Nkx-2.5 response element, termed the NKE, in the proximal region of the cardiac atrial natriuretic factor (ANF) promoter. The NKE is composed of two near-consensus NK2 binding sites that are each able to bind purified Nkx-2.5. The NKE is sufficient to confer cardiac cell-specific activity to a minimal TATA-containing promoter and is required for Nkx-2.5 activation of the ANF promoter in heterologous cells. Interestingly, in primary cardiocyte cultures, the NKE contributes to ANF promoter activity in a chamber- and developmental stage-specific manner, suggesting that Nkx-2.5 and/or other related cardiac proteins may play a role in chamber specification. This work provides the identification of a direct target for NK2 homeoproteins in the heart and lays the foundation for further molecular analyses of the role of Nkx-2.5 and other NK2 proteins in cardiac development.
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- Acebrón A., Aza-Blanc P., Rossi D. L., Lamas L., Santisteban P. Congenital human thyroglobulin defect due to low expression of the thyroid-specific transcription factor TTF-1. J Clin Invest. 1995 Aug;96(2):781–785. doi: 10.1172/JCI118123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ardati A., Nemer M. A nuclear pathway for alpha 1-adrenergic receptor signaling in cardiac cells. EMBO J. 1993 Dec 15;12(13):5131–5139. doi: 10.1002/j.1460-2075.1993.tb06208.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Argentin S., Ardati A., Tremblay S., Lihrmann I., Robitaille L., Drouin J., Nemer M. Developmental stage-specific regulation of atrial natriuretic factor gene transcription in cardiac cells. Mol Cell Biol. 1994 Jan;14(1):777–790. doi: 10.1128/mcb.14.1.777. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Argentin S., Nemer M., Drouin J., Scott G. K., Kennedy B. P., Davies P. L. The gene for rat atrial natriuretic factor. J Biol Chem. 1985 Apr 25;260(8):4568–4571. [PubMed] [Google Scholar]
- Azpiazu N., Frasch M. tinman and bagpipe: two homeo box genes that determine cell fates in the dorsal mesoderm of Drosophila. Genes Dev. 1993 Jul;7(7B):1325–1340. doi: 10.1101/gad.7.7b.1325. [DOI] [PubMed] [Google Scholar]
- Bodmer R. The gene tinman is required for specification of the heart and visceral muscles in Drosophila. Development. 1993 Jul;118(3):719–729. doi: 10.1242/dev.118.3.719. [DOI] [PubMed] [Google Scholar]
- Bohinski R. J., Di Lauro R., Whitsett J. A. The lung-specific surfactant protein B gene promoter is a target for thyroid transcription factor 1 and hepatocyte nuclear factor 3, indicating common factors for organ-specific gene expression along the foregut axis. Mol Cell Biol. 1994 Sep;14(9):5671–5681. doi: 10.1128/mcb.14.9.5671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen C. Y., Schwartz R. J. Identification of novel DNA binding targets and regulatory domains of a murine tinman homeodomain factor, nkx-2.5. J Biol Chem. 1995 Jun 30;270(26):15628–15633. doi: 10.1074/jbc.270.26.15628. [DOI] [PubMed] [Google Scholar]
- De Felice M., Damante G., Zannini M., Francis-Lang H., Di Lauro R. Redundant domains contribute to the transcriptional activity of the thyroid transcription factor 1. J Biol Chem. 1995 Nov 3;270(44):26649–26656. doi: 10.1074/jbc.270.44.26649. [DOI] [PubMed] [Google Scholar]
- Evans S. M., Yan W., Murillo M. P., Ponce J., Papalopulu N. tinman, a Drosophila homeobox gene required for heart and visceral mesoderm specification, may be represented by a family of genes in vertebrates: XNkx-2.3, a second vertebrate homologue of tinman. Development. 1995 Nov;121(11):3889–3899. doi: 10.1242/dev.121.11.3889. [DOI] [PubMed] [Google Scholar]
- Fabbro D., Tell G., Pellizzari L., Leonardi A., Pucillo C., Lonigro R., Damante G. Definition of the DNA-binding specificity of TTF-1 homeodomain by chromatographic selection of binding sequences. Biochem Biophys Res Commun. 1995 Aug 24;213(3):781–788. doi: 10.1006/bbrc.1995.2198. [DOI] [PubMed] [Google Scholar]
- Field L. J. Atrial natriuretic factor-SV40 T antigen transgenes produce tumors and cardiac arrhythmias in mice. Science. 1988 Feb 26;239(4843):1029–1033. doi: 10.1126/science.2964082. [DOI] [PubMed] [Google Scholar]
- Franz W. M., Breves D., Klingel K., Brem G., Hofschneider P. H., Kandolf R. Heart-specific targeting of firefly luciferase by the myosin light chain-2 promoter and developmental regulation in transgenic mice. Circ Res. 1993 Oct;73(4):629–638. doi: 10.1161/01.res.73.4.629. [DOI] [PubMed] [Google Scholar]
- Garcia-Fernàndez J., Baguñ J., Saló E. Genomic organization and expression of the planarian homeobox genes Dth-1 and Dth-2. Development. 1993 May;118(1):241–253. doi: 10.1242/dev.118.1.241. [DOI] [PubMed] [Google Scholar]
- Garcia-Fernàndez J., Baguñ J., Saló E. Planarian homeobox genes: cloning, sequence analysis, and expression. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7338–7342. doi: 10.1073/pnas.88.16.7338. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gehring W. J., Affolter M., Bürglin T. Homeodomain proteins. Annu Rev Biochem. 1994;63:487–526. doi: 10.1146/annurev.bi.63.070194.002415. [DOI] [PubMed] [Google Scholar]
- Gehring W. J., Qian Y. Q., Billeter M., Furukubo-Tokunaga K., Schier A. F., Resendez-Perez D., Affolter M., Otting G., Wüthrich K. Homeodomain-DNA recognition. Cell. 1994 Jul 29;78(2):211–223. doi: 10.1016/0092-8674(94)90292-5. [DOI] [PubMed] [Google Scholar]
- Grépin C., Dagnino L., Robitaille L., Haberstroh L., Antakly T., Nemer M. A hormone-encoding gene identifies a pathway for cardiac but not skeletal muscle gene transcription. Mol Cell Biol. 1994 May;14(5):3115–3129. doi: 10.1128/mcb.14.5.3115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guazzi S., Price M., De Felice M., Damante G., Mattei M. G., Di Lauro R. Thyroid nuclear factor 1 (TTF-1) contains a homeodomain and displays a novel DNA binding specificity. EMBO J. 1990 Nov;9(11):3631–3639. doi: 10.1002/j.1460-2075.1990.tb07574.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ip H. S., Wilson D. B., Heikinheimo M., Tang Z., Ting C. N., Simon M. C., Leiden J. M., Parmacek M. S. The GATA-4 transcription factor transactivates the cardiac muscle-specific troponin C promoter-enhancer in nonmuscle cells. Mol Cell Biol. 1994 Nov;14(11):7517–7526. doi: 10.1128/mcb.14.11.7517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jiménez F., Martin-Morris L. E., Velasco L., Chu H., Sierra J., Rosen D. R., White K. vnd, a gene required for early neurogenesis of Drosophila, encodes a homeodomain protein. EMBO J. 1995 Jul 17;14(14):3487–3495. doi: 10.1002/j.1460-2075.1995.tb07355.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson J. E., Wold B. J., Hauschka S. D. Muscle creatine kinase sequence elements regulating skeletal and cardiac muscle expression in transgenic mice. Mol Cell Biol. 1989 Aug;9(8):3393–3399. doi: 10.1128/mcb.9.8.3393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kelly R., Alonso S., Tajbakhsh S., Cossu G., Buckingham M. Myosin light chain 3F regulatory sequences confer regionalized cardiac and skeletal muscle expression in transgenic mice. J Cell Biol. 1995 Apr;129(2):383–396. doi: 10.1083/jcb.129.2.383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kim Y., Nirenberg M. Drosophila NK-homeobox genes. Proc Natl Acad Sci U S A. 1989 Oct;86(20):7716–7720. doi: 10.1073/pnas.86.20.7716. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kimura S., Hara Y., Pineau T., Fernandez-Salguero P., Fox C. H., Ward J. M., Gonzalez F. J. The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary. Genes Dev. 1996 Jan 1;10(1):60–69. doi: 10.1101/gad.10.1.60. [DOI] [PubMed] [Google Scholar]
- Komuro I., Izumo S. Csx: a murine homeobox-containing gene specifically expressed in the developing heart. Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8145–8149. doi: 10.1073/pnas.90.17.8145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liew C. C., Sole M. J., Yamauchi-Takihara K., Kellam B., Anderson D. H., Lin L. P., Liew J. C. Complete sequence and organization of the human cardiac beta-myosin heavy chain gene. Nucleic Acids Res. 1990 Jun 25;18(12):3647–3651. doi: 10.1093/nar/18.12.3647. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lints T. J., Parsons L. M., Hartley L., Lyons I., Harvey R. P. Nkx-2.5: a novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants. Development. 1993 Oct;119(2):419–431. doi: 10.1242/dev.119.2.419. [DOI] [PubMed] [Google Scholar]
- Lyons I., Parsons L. M., Hartley L., Li R., Andrews J. E., Robb L., Harvey R. P. Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5. Genes Dev. 1995 Jul 1;9(13):1654–1666. doi: 10.1101/gad.9.13.1654. [DOI] [PubMed] [Google Scholar]
- McBride K., Robitaille L., Tremblay S., Argentin S., Nemer M. fos/jun repression of cardiac-specific transcription in quiescent and growth-stimulated myocytes is targeted at a tissue-specific cis element. Mol Cell Biol. 1993 Jan;13(1):600–612. doi: 10.1128/mcb.13.1.600. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miwa T., Kedes L. Duplicated CArG box domains have positive and mutually dependent regulatory roles in expression of the human alpha-cardiac actin gene. Mol Cell Biol. 1987 Aug;7(8):2803–2813. doi: 10.1128/mcb.7.8.2803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Molkentin J. D., Brogan R. S., Jobe S. M., Markham B. E. Expression of the alpha-myosin heavy chain gene in the heart is regulated in part by an E-box-dependent mechanism. J Biol Chem. 1993 Feb 5;268(4):2602–2609. [PubMed] [Google Scholar]
- Molkentin J. D., Kalvakolanu D. V., Markham B. E. Transcription factor GATA-4 regulates cardiac muscle-specific expression of the alpha-myosin heavy-chain gene. Mol Cell Biol. 1994 Jul;14(7):4947–4957. doi: 10.1128/mcb.14.7.4947. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Molkentin J. D., Markham B. E. An M-CAT binding factor and an RSRF-related A-rich binding factor positively regulate expression of the alpha-cardiac myosin heavy-chain gene in vivo. Mol Cell Biol. 1994 Aug;14(8):5056–5065. doi: 10.1128/mcb.14.8.5056. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moss J. B., McQuinn T. C., Schwartz R. J. The avian cardiac alpha-actin promoter is regulated through a pair of complex elements composed of E boxes and serum response elements that bind both positive- and negative-acting factors. J Biol Chem. 1994 Apr 29;269(17):12731–12740. [PubMed] [Google Scholar]
- Nardelli-Haefliger D., Shankland M. Lox10, a member of the NK-2 homeobox gene class, is expressed in a segmental pattern in the endoderm and in the cephalic nervous system of the leech Helobdella. Development. 1993 Jul;118(3):877–892. doi: 10.1242/dev.118.3.877. [DOI] [PubMed] [Google Scholar]
- Navankasattusas S., Zhu H., Garcia A. V., Evans S. M., Chien K. R. A ubiquitous factor (HF-1a) and a distinct muscle factor (HF-1b/MEF-2) form an E-box-independent pathway for cardiac muscle gene expression. Mol Cell Biol. 1992 Apr;12(4):1469–1479. doi: 10.1128/mcb.12.4.1469. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nudel U., Calvo J. M., Shani M., Levy Z. The nucleotide sequence of a rat myosin light chain 2 gene. Nucleic Acids Res. 1984 Sep 25;12(18):7175–7186. doi: 10.1093/nar/12.18.7175. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Okkema P. G., Fire A. The Caenorhabditis elegans NK-2 class homeoprotein CEH-22 is involved in combinatorial activation of gene expression in pharyngeal muscle. Development. 1994 Aug;120(8):2175–2186. doi: 10.1242/dev.120.8.2175. [DOI] [PubMed] [Google Scholar]
- Otting G., Qian Y. Q., Billeter M., Müller M., Affolter M., Gehring W. J., Wüthrich K. Protein--DNA contacts in the structure of a homeodomain--DNA complex determined by nuclear magnetic resonance spectroscopy in solution. EMBO J. 1990 Oct;9(10):3085–3092. doi: 10.1002/j.1460-2075.1990.tb07505.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Parsons W. J., Richardson J. A., Graves K. H., Williams R. S., Moreadith R. W. Gradients of transgene expression directed by the human myoglobin promoter in the developing mouse heart. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1726–1730. doi: 10.1073/pnas.90.5.1726. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Price M., Lazzaro D., Pohl T., Mattei M. G., Rüther U., Olivo J. C., Duboule D., Di Lauro R. Regional expression of the homeobox gene Nkx-2.2 in the developing mammalian forebrain. Neuron. 1992 Feb;8(2):241–255. doi: 10.1016/0896-6273(92)90291-k. [DOI] [PubMed] [Google Scholar]
- Qasba P., Lin E., Zhou M. D., Kumar A., Siddiqui M. A. A single transcription factor binds to two divergent sequence elements with a common function in cardiac myosin light chain-2 promoter. Mol Cell Biol. 1992 Mar;12(3):1107–1116. doi: 10.1128/mcb.12.3.1107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rindt H., Gulick J., Knotts S., Neumann J., Robbins J. In vivo analysis of the murine beta-myosin heavy chain gene promoter. J Biol Chem. 1993 Mar 5;268(7):5332–5338. [PubMed] [Google Scholar]
- Scott M. P., Tamkun J. W., Hartzell G. W., 3rd The structure and function of the homeodomain. Biochim Biophys Acta. 1989 Jul 28;989(1):25–48. doi: 10.1016/0304-419x(89)90033-4. [DOI] [PubMed] [Google Scholar]
- Seidman C. E., Schmidt E. V., Seidman J. G. cis-dominance of rat atrial natriuretic factor gene regulatory sequences in transgenic mice. Can J Physiol Pharmacol. 1991 Oct;69(10):1486–1492. doi: 10.1139/y91-223. [DOI] [PubMed] [Google Scholar]
- Stewart A. F., Larkin S. B., Farrance I. K., Mar J. H., Hall D. E., Ordahl C. P. Muscle-enriched TEF-1 isoforms bind M-CAT elements from muscle-specific promoters and differentially activate transcription. J Biol Chem. 1994 Feb 4;269(5):3147–3150. [PubMed] [Google Scholar]
- Tonissen K. F., Drysdale T. A., Lints T. J., Harvey R. P., Krieg P. A. XNkx-2.5, a Xenopus gene related to Nkx-2.5 and tinman: evidence for a conserved role in cardiac development. Dev Biol. 1994 Mar;162(1):325–328. doi: 10.1006/dbio.1994.1089. [DOI] [PubMed] [Google Scholar]
- Vincent C. K., Gualberto A., Patel C. V., Walsh K. Different regulatory sequences control creatine kinase-M gene expression in directly injected skeletal and cardiac muscle. Mol Cell Biol. 1993 Feb;13(2):1264–1272. doi: 10.1128/mcb.13.2.1264. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zeller R., Bloch K. D., Williams B. S., Arceci R. J., Seidman C. E. Localized expression of the atrial natriuretic factor gene during cardiac embryogenesis. Genes Dev. 1987 Sep;1(7):693–698. doi: 10.1101/gad.1.7.693. [DOI] [PubMed] [Google Scholar]