Evidence map›Paper›PMID 31408468›Full record

ArticlePloS one2019

The genomic landscape of estrogen receptor α binding sites in mouse mammary gland.

Murugesan Palaniappan, Loc Nguyen, Sandra L Grimm, Yuanxin Xi, Zheng Xia, Wei Li, Cristian Coarfa

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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
4.1field-weighted citation impact, top 6% 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, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. FOXM1 cooperates with ERα to regulate functional β-cell mass.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Estrogen Receptor Alpha and ESR1 Mutations in Breast Cancer.Advances in experimental medicine and biology · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  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 1 institution in 1 country.

Murugesan PalaniappanDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, United States of America.ORCID 0000-0003-4916-6565
Loc NguyenDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, United States of America.
Sandra L GrimmDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, United States of America.
Yuanxin XiDivision of Biostatistics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, United States of America.
Zheng XiaDivision of Biostatistics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, United States of America.
Wei LiDivision of Biostatistics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, United States of America.
Cristian CoarfaDan L. Duncan Cancer Center, Baylor College of Medicine, Houston, United States of America.
Baylor College of Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptor α (ERα) is the major driving transcription factor in the mammary gland development as well as breast cancer initiation and progression. However, the genomic landscape of ERα binding sites in the normal mouse mammary gland has not been completely elucidated. Here, we mapped genome-wide ERα binding events by chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) in the mouse mammary gland in response to estradiol. We identified 6237 high confidence ERα binding sites in two biological replicates and showed that many of these were located at distal enhancer regions. Furthermore, we discovered 3686 unique genes in the mouse genome that recruit ER in response to estradiol. Interrogation of ER-DNA binding sites in ER-positive luminal epithelial cells showed that the ERE, PAX2, SF1, and AP1 motifs were highly enriched at distal enhancer regions. In addition, comprehensive transcriptome analysis by RNA-seq revealed that 493 genes are differentially regulated by acute treatment with estradiol in the mouse mammary gland in vivo. Through integration of RNA-seq and ERα ChIP-seq data, we uncovered a novel ERα targetome in mouse mammary epithelial cells. Taken together, our study has identified the genomic landscape of ERα binding events in mouse mammary epithelial cells. Furthermore, our study also highlights the cis-regulatory elements and cofactors that are involved in estrogen signaling and may contribute to ductal elongation in the normal mouse mammary gland.

Indexed as

AnimalsBinding SitesChromatin ImmunoprecipitationEstrogen Receptor alphaFemaleGene Expression ProfilingGenome-Wide Association StudyGenomicsHigh-Throughput Nucleotide SequencingMammary Glands, AnimalMiceReal-Time Polymerase Chain ReactionEstrogen Receptor alpha

Identifiers

PMID31408468
PMCPMC6692022
OpenAlexW2973172290

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.