TY - CHAP
T1 - Use of Gene-Manipulated Mice in the Study of Erythropoietin Gene Expression
AU - Suzuki, Norio
AU - Obara, Naoshi
AU - Yamamoto, Masayuki
N1 - Funding Information:
We thank Drs. Jon Maher, Mikiko Suzuki, and Shigehiko Imagawa (University of Tsukuba) and Dr. Yoshiaki Kondo (Tohoku University) for their help and stimulating discussions. This work is supported in part by the Japan Science and Technology Agency through the ERATO Environmental Response Project.
PY - 2007
Y1 - 2007
N2 - Transcriptional regulation of animal genes has been classified into two major categories: tissue-specific and stress-inducible. Erythropoietin (EPO), an erythroid growth factor, plays a central role in the regulation of red blood cell production. In response to hypoxic and/or anemic stresses, Epo gene expression is markedly induced in kidney and liver; thus, the Epo gene has been used as a model for elucidating stress-inducible gene expression in animals. A key transcriptional regulator of the hypoxia response, hypoxia-inducible transcription factor (HIF), has been identified and cloned through studies on the Epo gene. Recently developed gene-modified mouse lines have proven to be a powerful means of exploring the regulatory mechanisms as well as the physiological significance of the tissue-specific and hypoxia-inducible expression of the Epo gene. In this chapter, several gene-modified mouse lines related to EPO and the EPO receptor are introduced, with emphasis placed on the examination of in vivo EPO activity, EPO function in nonhematopoietic tissues, EPO-producing cells in the kidney, and cis-acting regulatory elements for Epo gene expression. These in vivo studies of the Epo gene have allowed for a deeper understanding of transcriptional regulation operated in a tissue-specific and stress-inducible manner.
AB - Transcriptional regulation of animal genes has been classified into two major categories: tissue-specific and stress-inducible. Erythropoietin (EPO), an erythroid growth factor, plays a central role in the regulation of red blood cell production. In response to hypoxic and/or anemic stresses, Epo gene expression is markedly induced in kidney and liver; thus, the Epo gene has been used as a model for elucidating stress-inducible gene expression in animals. A key transcriptional regulator of the hypoxia response, hypoxia-inducible transcription factor (HIF), has been identified and cloned through studies on the Epo gene. Recently developed gene-modified mouse lines have proven to be a powerful means of exploring the regulatory mechanisms as well as the physiological significance of the tissue-specific and hypoxia-inducible expression of the Epo gene. In this chapter, several gene-modified mouse lines related to EPO and the EPO receptor are introduced, with emphasis placed on the examination of in vivo EPO activity, EPO function in nonhematopoietic tissues, EPO-producing cells in the kidney, and cis-acting regulatory elements for Epo gene expression. These in vivo studies of the Epo gene have allowed for a deeper understanding of transcriptional regulation operated in a tissue-specific and stress-inducible manner.
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U2 - 10.1016/S0076-6879(07)35009-X
DO - 10.1016/S0076-6879(07)35009-X
M3 - Chapter
C2 - 17998054
AN - SCOPUS:39749200886
SN - 9780123739704
T3 - Methods in Enzymology
SP - 157
EP - 177
BT - Oxygen Biology and Hypoxia
A2 - Sies, Helmut
A2 - Brune, Bernhard
ER -