Evidence map›Paper›PMID 27729432›Full record

ArticleG3 (Bethesda, Md.)2016

Analysis of a lin-42/period Null Allele Implicates All Three Isoforms in Regulation of Caenorhabditis elegans Molting and Developmental Timing.

Theresa L B Edelman, Katherine A McCulloch, Angela Barr, Christian Frøkjær-Jensen, Erik M Jorgensen, Ann E Rougvie

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Temporal scaling inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Natural alleles of the clock geneFrontiers in physiology · 2022
    Article
  12. Article
  13. The Doubletime HomologG3 (Bethesda, Md.) · 2018
    Article
  14. Molting inWorm · 2017
    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

6 authors at 2 institutions in 1 country.

Theresa L B EdelmanDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55454.
Katherine A McCullochDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55454.
Angela BarrDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55454.
Christian Frøkjær-JensenDepartment of Biology, Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112.
Erik M JorgensenDepartment of Biology, Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112.
Ann E RougvieDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55454 rougvie@umn.edu.
University of Minnesota · USHoward Hughes Medical Institute · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Engineering the C. Elegans GenomeR01GM095817 · NIGMS · UNIVERSITY OF UTAH · PI JORGENSEN, ERIK M · 2011 to 2021
$2.8M
TEMPORAL CONTROL OF DEVELOPMENT IN C ELEGANSR01GM050227 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ROUGVIE, ANN E. · 1997 to 2010
$2.5M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007480 · NICHD · UNIVERSITY OF MINNESOTA TWIN CITIES · PI O'CONNOR, MICHAEL BRENDAN · 1995 to 2011
$1.2M
NICHD NIH HHS T32 HD007480NIGMS NIH HHS R01 GM050227NIGMS NIH HHS R01 GM095817NIH HHS P40 OD010440
6 · The paper itself

Abstract

The Caenorhabditis elegans heterochronic gene pathway regulates the relative timing of events during postembryonic development. lin-42, the worm homolog of the circadian clock gene, period, is a critical element of this pathway. lin-42 function has been defined by a set of hypomorphic alleles that cause precocious phenotypes, in which later developmental events, such as the terminal differentiation of hypodermal cells, occur too early. A subset of alleles also reveals a significant role for lin-42 in molting; larval stages are lengthened and ecdysis often fails in these mutant animals. lin-42 is a complex locus, encoding overlapping and nonoverlapping isoforms. Although existing alleles that affect subsets of isoforms have illuminated important and distinct roles for this gene in developmental timing, molting, and the decision to enter the alternative dauer state, it is essential to have a null allele to understand all of the roles of lin-42 and its individual isoforms. To remedy this problem and discover the null phenotype, we engineered an allele that deletes the entire lin-42 protein-coding region. lin-42 null mutants are homozygously viable, but have more severe phenotypes than observed in previously characterized hypomorphic alleles. We also provide additional evidence for this conclusion by using the null allele as a base for reintroducing different isoforms, showing that each isoform can provide heterochronic and molting pathway activities. Transcript levels of the nonoverlapping isoforms appear to be under coordinate temporal regulation, despite being driven by independent promoters. The lin-42 null allele will continue to be an important tool for dissecting the functions of lin-42 in molting and developmental timing.

Indexed as

AllelesGene Expression Regulation, DevelopmentalGenotypeAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsGenetic LociMoltingPenetrancePhenotypeProtein IsoformsTranscription FactorsTranscription, GeneticCaenorhabditis elegans ProteinsLIN-42 protein, C elegansProtein IsoformsTranscription FactorsCaenorhabditis elegansheterochronylin-42molting

Identifiers

PMID27729432
PMCPMC5144976
OpenAlexW2537388355

What OpenQuestion holds

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LicenceCC BY
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.