Evidence map›Paper›PMID 17199897›Full record

ArticleBMC developmental biology2007

Multiple upstream modules regulate zebrafish myf5 expression.

Yau-Hung Chen, Yun-Hsin Wang, Min-Yen Chang, Cheng-Yung Lin, Chih-Wei Weng, Monte Westerfield, Huai-Jen Tsai

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.4field-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

23 citing papers in PubMed, 166 citations in OpenAlex.

  1. Hb-EGF directs systemic muscle repair.Development (Cambridge, England) · 2026
    Article
  2. Review
  3. Article
  4. Fgf-driven Tbx protein activities directly induceDevelopment (Cambridge, England) · 2020
    Article
  5. Article
  6. Open biology · 2017
    Article
  7. Article
  8. Article
  9. Using Transgenic Zebrafish to Study Muscle Stem/Progenitor Cells.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

7 authors at 3 institutions in 2 countries.

Yau-Hung ChenGraduate Institute of Life Sciences, Tamkang University, Tamsui, Taiwan. yauhung@mail.tku.edu.tw <yauhung@mail.tku.edu.tw>
Yun-Hsin Wang
Min-Yen Chang
Cheng-Yung Lin
Chih-Wei Weng
Monte Westerfield
Huai-Jen Tsai
National Taiwan University · TWTamkang University · TWUniversity of Oregon · US

Funding

Zebrafish FacilityP01HD022486 · NICHD · UNIVERSITY OF OREGON · PI EISEN, JUDITH S · 1987 to 2017
$28.8M
SPECIFICATION OF MUSCLE CELL FATESR01AR045575 · NIAMS · UNIVERSITY OF OREGON · PI WESTERFIELD, MONTE · 1999 to 2008
$2.7M
NIAMS NIH HHS AR45575NIAMS NIH HHS R01 AR045575NICHD NIH HHS HD22486NICHD NIH HHS P01 HD022486
6 · The paper itself

Abstract

backgroundMyf5 is one member of the basic helix-loop-helix family of transcription factors, and it functions as a myogenic factor that is important for the specification and differentiation of muscle cells. The expression of myf5 is somite- and stage-dependent during embryogenesis through a delicate regulation. However, this complex regulatory mechanism of myf5 is not clearly understood.

resultsWe isolated a 156-kb bacterial artificial chromosome clone that includes an upstream 80-kb region and a downstream 70-kb region of zebrafish myf5 and generated a transgenic line carrying this 156-kb segment fused to a green fluorescent protein (GFP) reporter gene. We find strong GFP expression in the most rostral somite and in the presomitic mesoderm during segmentation stages, similar to endogenous myf5 expression. Later, the GFP signals persist in caudal somites near the tail bud but are down-regulated in the older, rostral somites. During the pharyngula period, we detect GFP signals in pectoral fin buds, dorsal rostral myotomes, hypaxial myotomes, and inferior oblique and superior oblique muscles, a pattern that also corresponds well with endogenous myf5 transcripts. To characterize the specific upstream cis-elements that regulate this complex and dynamic expression pattern, we also generated several transgenic lines that harbor various lengths within the upstream 80-kb segment. We find that (1) the -80 kb/-9977 segment contains a fin and cranial muscle element and a notochord repressor; (2) the -9977/-6213 segment contains a strong repressive element that does not include the notochord-specific repressor; (3) the -6212/-2938 segment contains tissue-specific elements for bone and spinal cord; (4) the -2937/-291 segment contains an eye enhancer, and the -2937/-2457 segment is required for notochord and myocyte expression; and (5) the -290/-1 segment is responsible for basal transcription in somites and the presomitic mesoderm.

conclusionWe suggest that the cell lineage-specific expression of myf5 is delicately orchestrated by multiple modules within the distal upstream region. This study provides an insight to understand the molecular control of myf5 and myogenesis in the zebrafish.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAnimals, Genetically ModifiedCloning, MolecularMyogenic Regulatory Factor 5Promoter Regions, GeneticUpstream Stimulatory FactorsZebrafishZebrafish ProteinsMyogenic Regulatory Factor 5Upstream Stimulatory FactorsZebrafish Proteins

Identifiers

PMID17199897
PMCPMC1769357
OpenAlexW1773194113

What OpenQuestion holds

Textmetadata
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.