Evidence map›Paper›PMID 24512688›Full record

ArticleDevelopmental biology2014

A role of the LIN-12/Notch signaling pathway in diversifying the non-striated egg-laying muscles in C. elegans.

Jared J Hale, Nirav M Amin, Carolyn George, Zachary Via, Herong Shi, Jun Liu

Abstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  4. Positive autoregulation ofDevelopment (Cambridge, England) · 2020
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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

6 authors at 1 institution in 1 country.

Jared J HaleDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, United States.
Nirav M AminDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, United States.
Carolyn GeorgeDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, United States.
Zachary ViaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, United States.
Herong ShiDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, United States.
Jun LiuDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, United States. Electronic address: JL53@cornell.edu.
Cornell University · US

Funding

PREDOCTORAL TRAINING IN GENETICS AND DEVELOPMENTT32GM007617 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BARBASH, DANIEL A · 1985 to 2021
$5.5M
Mesodermal Cell Fate Specification in C.elegansR01GM066953 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIU, JUN · 2002 to 2016
$3.9M
NIGMS NIH HHS R01 GM066953NIGMS NIH HHS R01GM066953NIGMS NIH HHS T32 GM007617
6 · The paper itself

Abstract

The proper formation and function of an organ is dependent on the specification and integration of multiple cell types and tissues. An example of this is the Caenorhabditis elegans hermaphrodite egg-laying system, which requires coordination between the vulva, uterus, neurons, and musculature. While the genetic constituents of the first three components have been well studied, little is known about the molecular mechanisms underlying the specification of the egg-laying musculature. The egg-laying muscles are non-striated in nature and consist of sixteen cells, four each of type I and type II vulval muscles and uterine muscles. These 16 non-striated muscles exhibit distinct morphology, location, synaptic connectivity and function. Using an RNAi screen targeting the putative transcription factors in the C. elegans genome, we identified a number of novel factors important for the diversification of these different types of egg-laying muscles. In particular, we found that RNAi knockdown of lag-1, which encodes the sole C. elegans ortholog of the transcription factor CSL (CBF1, Suppressor of Hairless, LAG-1), an effector of the LIN-12/Notch pathway, led to the production of extra type I vulval muscles. Similar phenotypes were also observed in animals with down-regulation of the Notch receptor LIN-12 and its DSL (Delta, Serrate, LAG-2) ligand LAG-2. The extra type I vulval muscles in animals with reduced LIN-12/Notch signaling resulted from a cell fate transformation of type II vulval muscles to type I vulval muscles. We showed that LIN-12/Notch was activated in the undifferentiated type II vulval muscle cells by LAG-2/DSL that is likely produced by the anchor cell (AC). Our findings provide additional evidence highlighting the roles of LIN-12/Notch signaling in coordinating the formation of various components of the functional C. elegans egg-laying system. We also identify multiple new factors that play critical roles in the proper specification of the different types of egg-laying muscles.

Indexed as

Signal TransductionAnimalsBody PatterningCaenorhabditis elegansCaenorhabditis elegans ProteinsFemaleHermaphroditic OrganismsLigandsMaleMusclesOvipositionReceptors, NotchRNA InterferenceTranscription FactorsVulvaCaenorhabditis elegans ProteinsLigandsLin-12 protein, C elegansReceptors, NotchTranscription FactorsC. eleganslag-1lag-2lin-12MesodermNon-striated muscleNotchsel-12sel-8Vulval muscle

Identifiers

PMID24512688
PMCPMC3981933
OpenAlexW2065241610

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Registered trials

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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.