Evidence map›Paper›PMID 15564334›Full record

ArticleEndocrinology2005

Preservation of eumelanin hair pigmentation in proopiomelanocortin-deficient mice on a nonagouti (a/a) genetic background.

Andrzej Slominski, Przemyslaw M Plonka, Alexander Pisarchik, James L Smart, Virginie Tolle, Jacobo Wortsman, Malcolm J Low

Abstract read
In one paragraph

Article in Endocrinology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

7 authors.

Andrzej SlominskiDepartment of Pathology and Laboratory Medicine, University of Tennessee, Memphis, Tennessee 38163, USA.
Przemyslaw M Plonka
Alexander Pisarchik
James L Smart
Virginie Tolle
Jacobo Wortsman
Malcolm J Low

Funding

Neurochemistry/Physiology of Proopiomelanocortin NeuronsR01DK066604 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOW, MALCOLM JAMES · 2004 to 2019
$5.2M
Role of CRH in skin physiology and pathologyR01AR047079 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SLOMINSKI, ANDRZEJ T · 2002 to 2004
$708k
Neurochemistry/physiology of proopiomelancortin neuronsR56DK066604 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI LOW, MALCOLM JAMES · 2008 to 2008
$267k
CONDITIONAL GENE TARGETING OF POMC IN THE HYPOTHALAMUSF31HG000201 · NHGRI · OREGON HEALTH AND SCIENCE UNIVERSITY · PI SMART, JAMES L · 1998 to 2001
$46k
NHGRI NIH HHS F31 HG000201NHGRI NIH HHS HG00201NIAMS NIH HHS AR47079NIAMS NIH HHS R01 AR047079NIDDK NIH HHS DK66604NIDDK NIH HHS R01 DK066604NIDDK NIH HHS R56 DK066604
6 · The paper itself

Abstract

The original strain of proopiomelanocortin (POMC)-deficient mice (Pomc-/-) was generated by homologous recombination in 129X1/SvJ (A(w)/A(w))-derived embryonic stem cells using a targeting construct that deleted exon 3, encoding all the known functional POMC-derived peptides including alpha MSH, from the Pomc gene. Although these Pomc-/- mice exhibited adrenal hypoplasia and obesity similar to the syndrome of POMC deficiency in children, their agouti coat color was only subtly altered. To further investigate the mechanism of hair pigmentation in the absence of POMC peptides, we studied wild-type (Pomc+/+), heterozygous (Pomc+/-), and homozygous (Pomc-/-) mice on a nonagouti (a/a) 129;B6 hybrid genetic background. All three genotypes had similar black fur pigmentation with yellow hairs behind the ears, around the nipples, and in the perianal area characteristic of inbred C57BL/6 mice. Histologic and electron paramagnetic resonance spectrometry examination demonstrated that hair follicles in back skin of Pomc-/- mice developed with normal structure and eumelanin pigmentation; corresponding molecular analyses, however, excluded local production of alpha MSH and ACTH because neither Pomc nor putative Pomc pseudogene mRNAs were detected in the skin. Thus, 129;B6 Pomc null mutant mice produce abundant eumelanin hair pigmentation despite their congenital absence of melanocortin ligands. These results suggest that either the mouse melanocortin receptor 1 has sufficient basal activity to trigger and sustain eumelanogenesis in vivo or that redundant nonmelanocortin pathway(s) compensate for the melanocortin deficiency. Whereas the latter implies feedback control of melanogenesis, it is also possible that the two mechanisms operate jointly in hair follicles.

Indexed as

PigmentationAdrenal GlandsAllelesalpha-MSHAnimalsCrosses, GeneticDNA, ComplementaryElectron Spin Resonance SpectroscopyExonsGene DeletionHairHair ColorHeterozygoteHomozygoteMelaninsMicealpha-MSHDNA, ComplementaryeumelaninMelaninsPro-Opiomelanocortin

Identifiers

PMID15564334
PMCPMC1201461

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.