Regulation of calreticulin gene expression by calcium

Mathilde Waser, Nasrin Mesaeli, Charlotte Spencer, Marek Michalak

Research output: Contribution to journalArticle

112 Citations (Scopus)

Abstract

We have isolated and characterized a 12-kb mouse genomic DNA fragment containing the entire calreticulin gene and 2.14 kb of the promoter region. The mouse calreticulin gene consists of nine exons and eight introns, and it spans 4.2 kb of genomic DNA. A 1.8-kb fragment of the calreticulin promoter was subcloned into a reporter gene plasmid containing chloramphenicol acetyltransferase. This construct was then used in transient and stable transfection of NIH/3T3 cells. Treatment of transfected cells either with the Ca2+ ionophore A23187, or with the ER Ca2+-ATPase inhibitor thapsigargin, resulted in a five- to sevenfold increase of the expression of chloramphenicol acetyltransferase protein. Transactivation of the calreticulin promoter was also increased by fourfold in NIH/3T3 cells treated with bradykinin, a hormone that induces Ca2+ release from the intracellular Ca2+ stores. Analysis of the promoter deletion constructs revealed that A23187- and thapsigargin-responsive regions are confined to two regions (- 115 to -260 and -685 to -1,763) in the calreticulin promoter that contain the CCAAT nucleotide sequences. Northern blot analysis of cells treated with A23187, or with thapsigargin, revealed a fivefold increase in calreticulin mRNA levels. Thapsigargin also induced a fourfold increase in calreticulun protein levels. Importantly, we show by nuclear run-on transcription analysis that calreticulin gene transcription is increased in NIH/3T3 cells treated with A23187 and thapsigargin in vivo. This increase in gene expression required over 4 h of continuous incubation with the drugs and was also sensitive to treatment with cycloheximide, suggesting that it is dependent on protein synthesis. Changes in the concentration of extracellular and cytoplasmic Ca2+ did not affect the increased expression of the calreticulin gene. These studies suggest that stress response to the depletion of intracellular Ca2+ stores induces expression of the calreticulin gene in vitro and in vivo.

Original languageEnglish
Pages (from-to)547-557
Number of pages11
JournalJournal of Cell Biology
Volume138
Issue number3
DOIs
Publication statusPublished - 11 Aug 1997
Externally publishedYes

Fingerprint

Calreticulin
Gene Expression Regulation
Calcium
Thapsigargin
Calcimycin
NIH 3T3 Cells
Chloramphenicol O-Acetyltransferase
Gene Expression
Genes
Proteins
Calcium-Transporting ATPases
DNA
Ionophores
Bradykinin
Cycloheximide
Reporter Genes
Genetic Promoter Regions
Northern Blotting
Introns
Transcriptional Activation

ASJC Scopus subject areas

  • Cell Biology

Cite this

Regulation of calreticulin gene expression by calcium. / Waser, Mathilde; Mesaeli, Nasrin; Spencer, Charlotte; Michalak, Marek.

In: Journal of Cell Biology, Vol. 138, No. 3, 11.08.1997, p. 547-557.

Research output: Contribution to journalArticle

Waser, Mathilde ; Mesaeli, Nasrin ; Spencer, Charlotte ; Michalak, Marek. / Regulation of calreticulin gene expression by calcium. In: Journal of Cell Biology. 1997 ; Vol. 138, No. 3. pp. 547-557.
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