Evidence map›Paper›PMID 10037785›Full record

ArticleThe Journal of cell biology1999

Processing of endogenous pre-mRNAs in association with SC-35 domains is gene specific.

K P Smith, P T Moen, K L Wydner, J R Coleman, J B Lawrence

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

95 citing papers in PubMed, 192 citations in OpenAlex.

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  19. Genome organization around nuclear speckles.Current opinion in genetics & development · 2019
    Review
  20. Article

35 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

K P SmithDepartment of Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA.
P T Moen
K L Wydner
J R Coleman
J B Lawrence
Brown University · USUniversity of Massachusetts Chan Medical School · US

Funding

NIGMS NIH HHS GM 49254
6 · The paper itself

Abstract

Analysis of six endogenous pre-mRNAs demonstrates that localization at the periphery or within splicing factor-rich (SC-35) domains is not restricted to a few unusually abundant pre-mRNAs, but is apparently a more common paradigm of many protein-coding genes. Different genes are preferentially transcribed and their RNAs processed in different compartments relative to SC-35 domains. These differences do not simply correlate with the complexity, nuclear abundance, or position within overall nuclear space. The distribution of spliceosome assembly factor SC-35 did not simply mirror the distribution of individual pre-mRNAs, but rather suggested that individual domains contain both specific pre-mRNA(s) as well as excess splicing factors. This is consistent with a multifunctional compartment, to which some gene loci and their RNAs have access and others do not. Despite similar molar abundance in muscle fiber nuclei, nascent transcript "trees" of highly complex dystrophin RNA are cotranscriptionally spliced outside of SC-35 domains, whereas posttranscriptional "tracks" of more mature myosin heavy chain transcripts overlap domains. Further analyses supported that endogenous pre-mRNAs exhibit distinct structural organization that may reflect not only the expression and complexity of the gene, but also constraints of its chromosomal context and kinetics of its RNA metabolism.

Indexed as

RibonucleoproteinsCell LineDystrophinHumansIn Situ Hybridization, FluorescenceMyosin Heavy ChainsNuclear ProteinsRNA, MessengerRNA PrecursorsRNA Processing, Post-TranscriptionalRNA SplicingSerine-Arginine Splicing FactorsSpliceosomesTranscription, GeneticDystrophinMyosin Heavy ChainsNuclear ProteinsRibonucleoproteinsRNA, MessengerRNA PrecursorsSerine-Arginine Splicing FactorsSRSF2 protein, human

Identifiers

PMID10037785
PMCPMC2132926
OpenAlexW2168879519

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC-SA
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.