Positive and negative cis-acting regulatory elements mediate expression of the mouse vascular smooth muscle α-actin gene

Douglas N. Foster, Bon Hong Min, Linda K. Foster, Elizabeth S. Stoflet, Siquan Sun, Michael J. Getz, Arthur R. Strauch

Research output: Contribution to journalArticle

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Abstract

Segments of the 5′-flanking region of the mouse vascular smooth muscle α-actin gene were assayed for promoter activity in transfected mouse BC3H1 myogenic cells and AKR-2B embryonic fibroblasts. The region between -150 and -191 that functions as a positive transcriptional element in myogenic and fibroblastic cells contains a mammalian-specific inverted CC(A/T)6GG-type consensus sequence. Expression was restricted to fully differentiated myogenic cells when an additional sequence spanning -191 to -224 was included in reporter gene constructs. This 33-base pair (bp) negative regulatory element is 70% conserved between the mouse and human genes and contains a 10-bp motif at its 3′ end that only partially resembles a CC(A/T)6GG element. Retention of a GGGA motif at the 3′ boundary of the 33-bp region is sufficient to maintain full transcriptional repression in fibroblasts and is partly responsible for repression in undifferentiated myoblasts. Complete muscle tissue-restrictive expression requires an additional 8 bp from the CC(A/ T)6GG-like element immediately 5′ to the GGGA motif, since replacement of this region with an unrelated 10-bp sequence completely eliminated restrictive transcriptional behavior in undifferentiated myoblasts. The distal portion of the 5′-flanking region between -224 and -1074 contains six E-box motifs (CANNTG) and mediates high level transcription only in postconfluent BC3H1 myoblasts. Analysis of reporter gene constructs including either the proximal E-box at -240 or all six E-boxes indicate that the five distal E-boxes are not required for high level transcription. A 724-bp segment of the 5′-flanking region consisting of the proximal E-box flanked upstream by a mammalianspecific 352-bp region was sufficient for maximal transcriptional activation in postconfluent BC3H1 myoblasts. Deletion of the 352-bp region restricts the early transcriptional response to high cell density in temporal studies of promoter activity during BC3H1 myogenic cell differentiation.

Original languageEnglish
Pages (from-to)11995-12003
Number of pages9
JournalJournal of Biological Chemistry
Volume267
Issue number17
Publication statusPublished - 1992 Jun 15
Externally publishedYes

Fingerprint

Vascular Smooth Muscle
Base Pairing
Muscle
Actins
5' Flanking Region
Genes
Myoblasts
Transcription
Fibroblasts
E-Box Elements
Reporter Genes
Chemical activation
Tissue
Time and Motion Studies
Consensus Sequence
Transcriptional Activation
Cell Differentiation
Cell Count
Muscles

ASJC Scopus subject areas

  • Biochemistry

Cite this

Foster, D. N., Min, B. H., Foster, L. K., Stoflet, E. S., Sun, S., Getz, M. J., & Strauch, A. R. (1992). Positive and negative cis-acting regulatory elements mediate expression of the mouse vascular smooth muscle α-actin gene. Journal of Biological Chemistry, 267(17), 11995-12003.

Positive and negative cis-acting regulatory elements mediate expression of the mouse vascular smooth muscle α-actin gene. / Foster, Douglas N.; Min, Bon Hong; Foster, Linda K.; Stoflet, Elizabeth S.; Sun, Siquan; Getz, Michael J.; Strauch, Arthur R.

In: Journal of Biological Chemistry, Vol. 267, No. 17, 15.06.1992, p. 11995-12003.

Research output: Contribution to journalArticle

Foster, DN, Min, BH, Foster, LK, Stoflet, ES, Sun, S, Getz, MJ & Strauch, AR 1992, 'Positive and negative cis-acting regulatory elements mediate expression of the mouse vascular smooth muscle α-actin gene', Journal of Biological Chemistry, vol. 267, no. 17, pp. 11995-12003.
Foster, Douglas N. ; Min, Bon Hong ; Foster, Linda K. ; Stoflet, Elizabeth S. ; Sun, Siquan ; Getz, Michael J. ; Strauch, Arthur R. / Positive and negative cis-acting regulatory elements mediate expression of the mouse vascular smooth muscle α-actin gene. In: Journal of Biological Chemistry. 1992 ; Vol. 267, No. 17. pp. 11995-12003.
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