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1.
Physiol Genomics ; 5(3): 137-45, 2001 Apr 02.
Artigo em Inglês | MEDLINE | ID: mdl-11285367

RESUMO

The cDNA of an uncoupling protein (UCP) homolog has been cloned from the swallow-tailed hummingbird, Eupetomena macroura. The hummingbird uncoupling protein (HmUCP) cDNA was amplified from pectoral muscle (flight muscle) using RT-PCR and primers for conserved domains of various known UCP homologs. The rapid amplification of cDNA ends (RACE) method was used to complete the cloning of the 5' and 3' ends of the open reading frame. The HmUCP coding region contains 915 nucleotides, and the deduced protein sequence consists of 304 amino acids, being approximately 72, 70, and 55% identical to human UCP3, UCP2, and UCP1, respectively. The uncoupling activity of this novel protein was characterized in yeast. In this expression system, the 12CA5-tagged HmUCP fusion protein was detected by Western blot in the enriched mitochondrial fraction. Similarly to rat UCP1, HmUCP decreased the mitochondrial membrane potential as measured in whole yeast by uptake of the fluorescent potential-sensitive dye 3',3-dihexyloxacarbocyanine iodide. The HmUCP mRNA is primarily expressed in skeletal muscle, but high levels can also be detected in heart and liver, as assessed by Northern blot analysis. Lowering the room's temperature to 12-14 degrees C triggered the cycle torpor/rewarming, typical of hummingbirds. Both in the pectoral muscle and heart, HmUCP mRNA levels were 1.5- to 3.4-fold higher during torpor. In conclusion, this is the first report of an UCP homolog in birds. The data indicate that HmUCP has the potential to function as an UCP and could play a thermogenic role during rewarming.


Assuntos
Aves/genética , Proteínas de Transporte/genética , Proteínas de Membrana/genética , Proteínas de Membrana Transportadoras , Proteínas Mitocondriais , Proteínas/genética , Sequência de Aminoácidos , Animais , Aves/fisiologia , Clonagem Molecular , Canais Iônicos , Potenciais da Membrana , Mitocôndrias/fisiologia , Dados de Sequência Molecular , Filogenia , RNA Mensageiro/biossíntese , Saccharomyces cerevisiae/fisiologia , Homologia de Sequência de Aminoácidos , Termogênese , Distribuição Tecidual , Proteína Desacopladora 1 , Proteína Desacopladora 2 , Proteína Desacopladora 3
2.
Int J Obes Relat Metab Disord ; 24(8): 1065-8, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10951548

RESUMO

OBJECTIVE: To investigate whether the region of chromosome 11 (11q13) containing the genes UCP2 and UCP3 could be excluded for linkage with a variety of obesity-related phenotypes in humans. DESIGN: Exclusion mapping using a variance component approach in extended pedigrees. SUBJECTS: Four-hundred and fifty eight individuals (195 females, 263 males) distributed in 10 Mexican American families of probands randomly ascertained with respect to any disease state and who are participating in the San Antonio Family Heart Study. Ages range from 18 to 87 (mean age 35 y). MEASUREMENTS: Serum leptin levels, fat mass (FM), body mass index (BMI), and waist circumference. RESULTS: We were able to exclude the chromosomal region containing UCP2/UCP3 as having an effect on this set of obesity-related phenotypes at relative effect sizes of 10% or greater (P-values<0.05). CONCLUSIONS: These results suggest that variation in these genes is unlikely to have a substantial effect on the expression of obesity-related phenotypes in the Mexican American population.


Assuntos
Proteínas de Transporte/genética , Cromossomos Humanos Par 11 , Proteínas de Membrana Transportadoras , Americanos Mexicanos/genética , Proteínas Mitocondriais , Obesidade/genética , Proteínas/genética , População Branca/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antropometria , Mapeamento Cromossômico , Feminino , Humanos , Canais Iônicos , Leptina/sangue , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Texas , Proteína Desacopladora 2 , Proteína Desacopladora 3
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