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פותח על ידי קלירמאש פתרונות בע"מ -
Quail MyoD Is Regulated by a Complex Array of cis-Acting Control Sequences
Year:
1995
Source of publication :
Developmental Biology
Authors :
פיירמן, אלכסנדר
;
.
שני, משה
;
.
Volume :
170
Co-Authors:
Pinney, D.F., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
de la Brousse, F.C., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Faerman, A., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Shani, M., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Maruyama, K., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Emerson Jr., C.P., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Facilitators :
From page:
21
To page:
38
(
Total pages:
18
)
Abstract:
Quail myoD (QmyoD) is the earliest myoD family member expressed in quail somites and its transcription is initiated in response to early developmental signals. We have investigated the transcriptional regulation of QmyoD to define the cis-acting sequences required for tissue-specific and correct developmental expression. The QmyoD gene locus was isolated and sequenced and its regulatory properties were characterized. We identified three distinct regions of cis-acting regulatory sequences that control the expression of reporter gene constructs following DNA transfection into cell lines and cultured primary quail cells. The first, a complex distal control region (DCR), 11.5 kb upstream of the gene, contains three separable enhancer activities. Two of these DCR enhancer activities are tissue specific and can be autoactivated. In addition, these same two enhancers and the entire DCR direct somite- and muscle-specific expression of a reporter gene in transgenic mice. Sequence analysis of the DCR enhancers reveals clusters of E-boxes, MEF2 binding motifs, and stretches of sequence identity with the human myoD enhancer. Second, the promoter region has sequences which act positively to direct expression in both muscle and nonmuscle cells as well as sequences that repress expression specifically in nonmuscle cells. The third control region, the PR, is located -3.3 to -5 kb from the transcription start site and directs muscle-specific expression in cultured cells. This analysis demonstrates that QmyoD has multiple control regions and that some features of myoD regulation are conserved between mammals and birds. © 1995 Academic Press. All rights reserved.
Note:
Related Files :
Animal
animal tissue
Base Sequence
cis acting element
genetic model
mice
Molecular Sequence Data
transcription factor
עוד תגיות
תוכן קשור
More details
DOI :
10.1006/dbio.1995.1192
Article number:
0
Affiliations:
Database:
סקופוס
Publication Type:
מאמר
;
.
Language:
אנגלית
Editors' remarks:
ID:
22525
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:52
Scientific Publication
Quail MyoD Is Regulated by a Complex Array of cis-Acting Control Sequences
170
Pinney, D.F., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
de la Brousse, F.C., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Faerman, A., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Shani, M., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Maruyama, K., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Emerson Jr., C.P., Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111 Institute of Animal Science, P.O. Box 6, Bet Dagan, 50250, Israel
Quail MyoD Is Regulated by a Complex Array of cis-Acting Control Sequences
Quail myoD (QmyoD) is the earliest myoD family member expressed in quail somites and its transcription is initiated in response to early developmental signals. We have investigated the transcriptional regulation of QmyoD to define the cis-acting sequences required for tissue-specific and correct developmental expression. The QmyoD gene locus was isolated and sequenced and its regulatory properties were characterized. We identified three distinct regions of cis-acting regulatory sequences that control the expression of reporter gene constructs following DNA transfection into cell lines and cultured primary quail cells. The first, a complex distal control region (DCR), 11.5 kb upstream of the gene, contains three separable enhancer activities. Two of these DCR enhancer activities are tissue specific and can be autoactivated. In addition, these same two enhancers and the entire DCR direct somite- and muscle-specific expression of a reporter gene in transgenic mice. Sequence analysis of the DCR enhancers reveals clusters of E-boxes, MEF2 binding motifs, and stretches of sequence identity with the human myoD enhancer. Second, the promoter region has sequences which act positively to direct expression in both muscle and nonmuscle cells as well as sequences that repress expression specifically in nonmuscle cells. The third control region, the PR, is located -3.3 to -5 kb from the transcription start site and directs muscle-specific expression in cultured cells. This analysis demonstrates that QmyoD has multiple control regions and that some features of myoD regulation are conserved between mammals and birds. © 1995 Academic Press. All rights reserved.
Scientific Publication
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