Skip Navigation

This Article
Right arrow Print PDF (2384K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (83)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Steiner, C.
Right arrow Articles by Renkawitz, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Steiner, C.
Right arrow Articles by Renkawitz, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1987, Vol. 15, No. 10 4163-4178
© 1987


Articles

Lysozyme gene activity in chicken macrophages is controlled by positive and negative regulatory elements

Christof Steiner, Marc Muller, Aria Baniahmad and Rainer Renkawitz

Max-Planck-Institut für Biochemie Genzentrum, D-8033 Martinsried, FRG

Received March 10, 1987. Accepted April 27, 1987.

The chicken lysozyme gene is constitutively active in macrophages and under the control of steroid hormones in the oviduct.To investigate which DNA elements are involved In the control of its expression in macrophages we performed transient DNA transfer experiments with two different types of plasmids: 5'-deletion mutants of the upstream region of the chicken lysozyme gene and different fragments from this area in front of the thymidine kinase promoter (herpes simplex virus), each placed in front of the CAT (chloramphenlcol acetyl transferase) coding sequence. Two enhancers (E-2.7kb and E-0.2kb) were characterized. They are active in macrophages, but not in chicken flbroblasts. Furthermore a negative element (N-2.4kb) was Identified, which is active in fibroblasts and promyelocytes, but not in mature macrophages. The combined action of all three elements contributes to the observed lysozyme gene activities: no activity In fibroblasts, moderate activity in promyelocytes and high activity in mature macrophages.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
O. Ivanova, D. Braas, and K.-H. Klempnauer
Oncogenic point mutations in the Myb DNA-binding domain alter the DNA-binding properties of Myb at a physiological target gene
Nucleic Acids Res., December 18, 2007; 35(21): 7237 - 7247.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
P. Lefevre, S. Melnik, N. Wilson, A. D. Riggs, and C. Bonifer
Developmentally Regulated Recruitment of Transcription Factors and Chromatin Modification Activities to Chicken Lysozyme cis-Regulatory Elements In Vivo
Mol. Cell. Biol., June 15, 2003; 23(12): 4386 - 4400.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
A. Heydemann, S. Warming, C. Clendenin, K. Sigrist, J. P. Hjorth, and M. C. Simon
A minimal c-fes cassette directs myeloid-specific expression in transgenic mice
Blood, November 1, 2000; 96(9): 3040 - 3048.
[Abstract] [Full Text] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
A.E. Sippel, G. Schafer, N. Faust, H. Saueressig, A. Hecht, and C. Bonifer
Chromatin Domains Constitute Regulatory Units for the Control of Eukaryotic Genes
Cold Spring Harb Symp Quant Biol, January 1, 1993; 58(0): 37 - 44.
[Abstract] [PDF]


Home page
ScienceHome page
R Schule, M Muller, C Kaltschmidt, and R Renkawitz
Many transcription factors interact synergistically with steroid receptors
Science, December 9, 1988; 242(4884): 1418 - 1420.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.