Evidence map›Paper›PMID 25694552›Full record

ArticleASN neuro

Control of human PLP1 expression through transcriptional regulatory elements and alternatively spliced exons in intron 1.

Hamdan Hamdan, Neriman T Kockara, Lee Ann Jolly, Shirley Haun, Patricia A Wight

Open access · goldAbstract read
In one paragraph

Article in ASN neuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Frontiers in cellular neuroscience · 2022
    Article
  3. Article
  4. Article
  5. 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

5 authors at 1 institution in 1 country.

Hamdan HamdanDepartment of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Neriman T KockaraDepartment of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Lee Ann JollyDepartment of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Shirley HaunDepartment of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Patricia A WightDepartment of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR, USA pwight@uams.edu.
University of Arkansas for Medical Sciences · US

Funding

ANTISILENCING OF PLP GENE EXPRESSION IN OLIGODENDROCYTESR01NS037821 · NINDS · UNIV OF ARKANSAS FOR MED SCIS · PI WIGHT, PATRICIA A. · 1998 to 2010
$2.0M
NINDS NIH HHS R01 NS037821
6 · The paper itself

Abstract

Although the myelin proteolipid protein gene (PLP1) encodes the most abundant protein in central nervous system (CNS) myelin, not much is known about the mechanisms that govern expression of the human gene (hPLP1). Much more is known about the processes that regulate Plp1 gene expression in rodents. From studies with Plp1-lacZ transgenic mice, it was determined that the first intron of mouse Plp1 (mPlp1) is required to attain high levels of expression in brain, concurrent with the active myelination period. Other studies have suggested that within mPlp1 intron 1 (>8 kb) lie several regions with enhancer-like activity. To test whether these sequences (and possibly others) in hPLP1 intron 1 are functional, deletion-transfection analysis was performed with hPLP1-lacZ constructs that contain various portions of the intron, or lack it altogether. Results presented here demonstrate the importance of hPLP1 intron 1 in achieving maximal levels of expression in the immortalized oligodendroglial cell line, Oli-neu. Deletion analysis indicates that the intron contains multiple positive regulatory elements which are active in Oli-neu cells. Some of these elements appear to be functionally conserved between human and mouse, while others are not. Furthermore, our studies demonstrate that multiple splice variants can be formed due to inclusion of extra (supplementary) exons from what is classically thought of as hPLP1 intron 1. Thus, splicing of these novel exons (which are not recognized as such in mPlp1 due to lack of conserved splice sites) must utilize factors common to both human and mouse since Oli-neu cells are of mouse origin.

Indexed as

Analysis of VarianceAnimalsCell Line, TransformedDNA, RecombinantExonsHumansLac OperonMiceMyelin Proteolipid ProteinOligodendrogliaRegulatory Elements, TranscriptionalTransfectionDNA, RecombinantMyelin Proteolipid ProteinPLP1 protein, humanenhancergene regulationmyelin proteolipid proteinOli-neu cellsRT-PCRsplice variants

Identifiers

PMID25694552
PMCPMC4342368
OpenAlexW2147471189

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.