Evidence map›Paper›PMID 11238888›Full record

ArticleMolecular and cellular biology2001

An upstream AG determines whether a downstream AG is selected during catalytic step II of splicing.

K Chua, R Reed

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

56 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
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  6. Characterization of a novel deep-intronic variant inCold Spring Harbor molecular case studies · 2022
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  15. Evolution of Alternative Splicing in Eudicots.Frontiers in plant science · 2019
    Article
  16. A birth of bipartite exon by intragenic deletion.Molecular genetics & genomic medicine · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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.

K ChuaDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
R Reed
Harvard University · US

Funding

MECHANISMS OF PREMRNA SPLICING IN HIGHER EUKARYOTESR01GM043375 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI REED, ROBIN E. · 1990 to 2015
$12.6M
Functional Coupling of Steps in Genes ExpressionR56GM043375 · NIGMS · HARVARD MEDICAL SCHOOL · PI REED, ROBIN E · 2007 to 2007
$563k
NIGMS NIH HHS GM 43375-11NIGMS NIH HHS R01 GM043375NIGMS NIH HHS R56 GM043375
6 · The paper itself

Abstract

Specific mechanisms must exist to ensure fidelity in selecting the AG dinucleotide that functions as the 3' splice site during the second transesterification step of splicing. Here we show that the optimal location for this AG is within a narrow distance (19 to 23 nucleotides [nt]) downstream from the branch point sequence (BPS). Contrary to previous expectations, AGs located less than 23 nt from the BPS are always recognized, even when a second AG located more optimally downstream is used in the transesterification reaction. Indeed, the AG closest to the BPS actually dictates the precise location of the AG that engages in the reaction. This mechanism, in which the AG is identified by a general localization step followed by a precise localization step, may be used to achieve fidelity while allowing flexibility in the location of 3' splice sites.

Indexed as

RNA Splice SitesCell NucleusModels, BiologicalNucleotidesPlasmidsRNA PrecursorsRNA SplicingNucleotidesRNA PrecursorsRNA Splice Sites

Identifiers

PMID11238888
PMCPMC86697
OpenAlexW2107402138

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.