Evidence map›Paper›PMID 21552418›Full record

ArticleInternational journal of biological sciences2011

Identification and characterization of the alternatively spliced nuclear receptor coactivator-6 isoforms.

Qingtian Li, Jianming Xu

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2011. 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
1.0field-weighted citation impact, top 21% 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, 12 citations in OpenAlex.

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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

2 authors at 2 institutions in 2 countries.

Qingtian LiDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Jianming Xu
Baylor College of Medicine · USSouthwest Medical University · CN

Funding

TISSUE COACTIVATOR AND RECEPTOR EXPRESSION FINGERPRINTSP01DK059820 · NIDDK · INSTITUT DE GENETIQUE ET BIOLOGIE MOLECU · PI TSAI, SOPHIA Y. · 2001 to 2016
$23.1M
The Role of SRC-1 in Breast CancerR01CA112403 · NCI · BAYLOR COLLEGE OF MEDICINE · PI XU, JIANMING · 2006 to 2016
$2.9M
Roles of SRC-3 in Development and DiseaseR01DK058242 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI XU, JIANMING · 2000 to 2013
$2.8M
Role of AIB3 in Mammary Gland and Breast CancerR01CA119689 · NCI · BAYLOR COLLEGE OF MEDICINE · PI XU, JIANMING · 2005 to 2009
$1.4M
NCI NIH HHS CA112403NCI NIH HHS CA119689NCI NIH HHS R01 CA112403NCI NIH HHS R01 CA119689NIDDK NIH HHS DK058242NIDDK NIH HHS DK59820NIDDK NIH HHS P01 DK059820NIDDK NIH HHS R01 DK058242
6 · The paper itself

Abstract

The nuclear receptor coactivator-6 (NCOA6, AIB3, PRIP, ASC-2, TRBP, RAP250 or NRC) is a co-activator for nuclear hormone receptors and certain other transcription factors. NCOA6 plays an important role in embryonic development, adipocyte differentiation, metabolism and breast carcinogenesis. The human and mouse NCOA6 genes had 15 and 14 previously identified exons, respectively. This study further identified an alternatively spliced exon 11b (E11b) in human or E10b in mouse, which codes a short polypeptide and a Stop codon, resulting in splicing variants lacking the last four exon-coded polypeptide. Analyses of mouse testis NCOA6 mRNAs identified four alternatively spliced variants, NCOA6-α (without E10b), -β (without E10a and E10b), -γ (with E10a and E10b) and -δ (without E10a but with E10b). These isoforms were detected in multiple mouse tissues and in MDA-MB-435 human cells. NCOA6-α and -β are mainly located in the nucleus; NCOA6-γ is located in both cytoplasm and nucleus; and NCOA6-δ is mainly located in mitochondria. The C-terminus coded by the last four exons was responsible for locating NCOA6-α and -β into the nucleus. The human E11a or mouse E10a-coded region is responsible for distributing NCOA6-γ in both cytoplasm and nucleus, while the region coded by E8-E9 in human or E7-E8 in mouse is responsible for directing NCOA6-δ to mitochondria. Our assays also demonstrated that NCOA6-α and -β could significantly enhance estrogen receptor α-mediated transcription, but NCOA6-γ and -δ were unable to do so. These results suggest that the diverse physiological function of NCOA6 may be mediated by multiple isoforms expressed in different tissues and localized in different subcellular compartments.

Indexed as

Alternative SplicingAnimalsHeLa CellsHumansMiceNuclear Receptor CoactivatorsProtein IsoformsReceptors, EstrogenRNA, MessengerSequence Analysis, DNATranscriptional ActivationNCOA6 protein, humanNcoa6 protein, mouseNuclear Receptor CoactivatorsProtein IsoformsReceptors, EstrogenRNA, MessengerNCOA6nuclear receptor coactivator-6

Identifiers

PMID21552418
PMCPMC3088874
OpenAlexW2165089977

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.