Evidence map›Paper›PMID 2524382›Full record

ArticleThe EMBO journal1989

Regulation of tissue-specific alternative splicing: exon-specific cis-elements govern the splicing of leukocyte common antigen pre-mRNA.

M Streuli, H Saito

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
8.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

55 citing papers in PubMed, 152 citations in OpenAlex.

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  19. Enhancement of antigen-induced T-cell proliferation by soluble CD26/dipeptidyl peptidase IV.Proceedings of the National Academy of Sciences of the United States of America · 1994
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

M StreuliDepartment of Pathology, Harvard Medical School, Boston, MA 02115.
H Saito
Harvard University · US

Funding

STRUCTURE AND FUNCTION OF LEUKOCYTE COMMON ANTIGENR01AI026598 · NIAID · DANA-FARBER CANCER INSTITUTE · PI SAITO, HARUO · 1988 to 1996
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NIAID NIH HHS AI-26598
6 · The paper itself

Abstract

Tissue-specific alternative splicing is an important mechanism for controlling gene expression. Exons 4, 5 and 6 of the human leukocyte common antigen (LCA) gene are included in B cell mRNA but excluded from thymocyte mRNA by differential splicing. In order to study this tissue-specific alternative splicing, we constructed mini-genes that contain only a few of the LCA exons and the SV40 promoter. Mouse B cells and thymocytes were transfected with these mini-gene constructs and the structures of mRNAs were determined by primer extension analysis. The results show that the same primary transcript is spliced alternatively in B cells and thymocytes. This finding suggests that there is a tissue-specific trans-acting factor that regulates the alternative splicing of LCA pre-mRNA. By making various deletion mutants, cis-elements necessary for tissue-specific splicing were confined within the alternatively spliced exons and their immediate flanking intron sequences. Furthermore, linker scanning analysis shows that there are at least three distinct cis-elements within the LCA exon 4 sequence that are required for tissue-specific alternative splicing. Possible mechanisms of LCA alternative splicing are discussed.

Indexed as

RNA SplicingAntigens, DifferentiationBase SequenceB-LymphocytesExonsGene Expression RegulationHistocompatibility AntigensHumansLeukocyte Common AntigensMolecular Sequence DataRNA PrecursorsTissue DistributionT-LymphocytesTranscription FactorsAntigens, DifferentiationHistocompatibility AntigensLeukocyte Common AntigensRNA PrecursorsTranscription Factors

Identifiers

PMID2524382
PMCPMC400875
OpenAlexW1750913658

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.