ArticleMolecular and cellular biology1993
Introns are essential for growth-regulated expression of the mouse thymidylate synthase gene.
Article in Molecular and cellular biology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 37 citations in OpenAlex.
- Inhibition of the mammalian transcription factor LSF induces S-phase-dependent apoptosis by downregulating thymidylate synthase expression.The EMBO journal · 2000Article
- Efficient 3'-end formation of human beta-globin mRNA in vivo requires sequences within the last intron but occurs independently of the splicing reaction.Nucleic acids research · 1998Article
- Regulated expression and RNA processing of transcripts from the Srp20 splicing factor gene during the cell cycle.Molecular and cellular biology · 1997Article
- Splicing signals are required for S-phase regulation of the mouse thymidylate synthase gene.Molecular and cellular biology · 1996Article
- Regulation of mouse thymidylate synthase gene expression in growth-stimulated cells: upstream S phase control elements are indistinguishable from the essential promoter elements.Nucleic acids research · 1995Article
- Bidirectional promoter of the mouse thymidylate synthase gene.Nucleic acids research · 1994Article
- New targets for pyrimidine antimetabolites in the treatment of solid tumours. 1: Thymidylate synthase.Pharmacy world & science : PWS · 1994Review
- Stimulation of gene expression by introns: conversion of an inhibitory intron to a stimulatory intron by alteration of the splice donor sequence.Nucleic acids research · 1993Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
The thymidylate synthase (TS) gene is expressed at much higher levels in proliferating cells than in quiescent cells. We have been studying the sequences that are important for regulating the mouse TS gene. We previously showed that DNA sequences upstream of the essential promoter elements as well as downstream of the ATG codon are both necessary (but neither is sufficient) for normal regulation in growth-stimulated cells. In the present study, we examined the possible roles of the coding region, polyadenylation signal, and introns as downstream regulatory elements. Minigenes consisting of 1 kb of the TS 5'-flanking region, the coding region (with or without various introns at their normal locations), and polyadenylation signals from the TS gene, the human beta-globin gene, and the bovine growth hormone gene were stably transfected into wild-type mouse 3T6 cells. Minigenes that contained introns 5 and 6, 1 and 2, or 1 alone were regulated regardless of which polyadenylation signal was included. A minigene that contained an internally deleted version of intron 1 was also regulated in response to growth stimulation. However, when all introns were omitted, there was little if any change in the level of minigene expression as cells progressed from G1 through S phase. These observations indicate that TS introns contain sequences that are necessary for normal growth-regulated expression of the mouse TS gene. These sequences appear to be associated with sequences that are important for splicing and to function in cooperation with upstream regulatory elements to bring about normal S-phase-specific expression.
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