Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Anim Biotechnol ; 31(2): 164-173, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30929567

RESUMO

Serine protease inhibitor protein 3 (serpin peptidase inhibitor, clade A, member 3, SERPINA3) is a member of the serpin superfamily, probably related to the yield and quality of muscle. This study focuses on the relationship between SERPINA3 gene polymorphism and growth traits in beef cattle. The study first uses sequencing pooled DNA samples (Pool-Seq), PCR-RFLP and Tetra-primer ARMS-PCR techniques to determine the genetic polymorphisms of SERPINA3 in 765 beef cattle. Then, the polymorphic loci were correlated with the growth characters of cattle. Five SNPs (SNP1:A-648G, SNP2:T6496A, SNP3:G2495A, SNP4:T2595A, SNP5:A2615G) were found, located in the promoter, introns 5 and SNP 3, 4, 5 were in exons 2, respectively. The observed He was from 0.44 to 0.5, Ne were approaching 2 (1.78 to 2.00). The maximum and minimum PIC (polymorphism information content) values were 0.37 and 0.34, respectively. The association analysis results showed that the SNPs had a significant height in the chest girth and body length. (p < 0.05 or p < 0.01). This will provide important information for the rapid breeding of Chinese yellow cattle and the establishment of a molecular genetic marker database.


Assuntos
Bovinos/genética , Regulação da Expressão Gênica/fisiologia , Serpinas/metabolismo , Animais , Bovinos/crescimento & desenvolvimento , DNA/genética , Marcadores Genéticos , Genótipo , Desequilíbrio de Ligação , Polimorfismo de Nucleotídeo Único , Serpinas/genética
2.
Anim Biotechnol ; 31(6): 532-537, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31280665

RESUMO

Copy number variation (CNV) is a form of genetic variation caused by genome rearrangement, with abnormal fragments ranging from 50 bp to Mb. And, CNV is closely related to disease, growth and reproductive shape of livestock. As a member of myosin light chain kinase (MYLK) family with serine/threonine specificity, MYLK4 belongs to an enzyme encoded by MYLK4 gene. Although MYLK4 is a recognized kinase, its function has yet to be revealed in subsequent studies. This study aims to analyze CNV and genetic effects of MYLK4 gene in goats. We used qPCR to detect CNV of MYLK4 gene in African Nubian goat (n = 32), Guizhou black goat (n = 196) and Guizhou white goat (n = 95), respectively, and correlated CNV data of MYLK4 gene with goat growth traits in Chinese goats. The results showed that the effect of MYLK4 gene CNV on body weight, body length and body height of goats had significantly different (p < 0.05, Q < 0.05), in which CNV showed better growth traits in type of deletion. Therefore, CNV of MYLK4 gene can be used as a molecular marker for assisted selection of goat growth traits, which provides a theoretical basis for the genetic improvement of goat breeds in China.


Assuntos
Variações do Número de Cópias de DNA/genética , Cabras/genética , Quinase de Cadeia Leve de Miosina/genética , Animais , Tamanho Corporal/genética , Marcadores Genéticos/genética , Cabras/crescimento & desenvolvimento
3.
Anim Biotechnol ; 31(1): 42-51, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-30570383

RESUMO

Cellular retinoic acid binding protein 2 (CRABP2) is essential to myoblast differentiation. However, there was no report about the function of CRABP2 gene in cattle. This study explored the association of CRABP2 gene polymorphisms with growth traits in cattle breeds by several methods, such as DNA sequencing, PCR, PCR-RFLP and forced PCR-RFLP. Two sequence variants were determined. There were 621 individuals in six cattle breeds from China for the experiment, and three breeds were used to test validation of polymorphisms and extent of linkage disequilibrium (LD). The results showed that both SNPs (SNP1, g.2458 G > T, SNP2, g.3878 G > A) were in intron1. Two SNPs were in low linkage disequilibrium. Association analysis suggested that SNP1 had the significant difference on growth traits with body height, height at hip cross and body slanting length (P < .05), while SNP2 showed a significant difference in growth traits with body height, height at hip cross and body slanting length(P < .05). The results of this investigation displayed that the CRABP2 gene is an available candidate gene and may be used for breed selection and conservation.


Assuntos
Bovinos/fisiologia , Estudos de Associação Genética/veterinária , Polimorfismo de Nucleotídeo Único/genética , Animais , Cruzamento , Bovinos/genética , Bovinos/crescimento & desenvolvimento , Feminino , Genótipo , Desequilíbrio de Ligação , Camundongos , Fenótipo , Polimorfismo de Fragmento de Restrição , Característica Quantitativa Herdável , Análise de Sequência de DNA/veterinária
4.
Arch Anim Breed ; 62(1): 171-179, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31807627

RESUMO

The insulin-like growth factor 1 receptor (IGF1R) plays a vital role in immunomodulation and muscle and bone growth. The copy number variation (CNV) is believed to the reason for many complex phenotypic variations. In this paper, we statistically analyzed the copy number and the expression profiling in different tissue types of the IGF1R gene using the 422 samples from four Chinese beef cattle breeds, and the mRNA of IGF1R was widely expressed in nine tissue types of adult cattle (heart, liver, kidney, muscle, fat, stomach, spleen, lung and testis). Results of CNV and growth traits indicated that the IGF1R CNV was significantly associated with body weight and body height of Jinnan (JN) cattle and was significantly associated with body height and hucklebone width of Qinchuan (QC) cattle, making IGF1R CNV a promising molecular marker to improve meat production in beef cattle breeding. Bioinformatics predictions show that the CNV region is highly similar to the human genome, and there are a large number of transcription factors, DNase I hypersensitive sites, and high levels of histone acetylation, suggesting that this region may play a role in transcriptional regulation, providing directions for further study of the role of bovine CNV and economic traits.

5.
Gene ; 680: 99-104, 2019 Jan 05.
Artigo em Inglês | MEDLINE | ID: mdl-30099021

RESUMO

Copy number variation (CNV) related to complex traits, such as disease and quantitative phenotype, is considered an important and wealthy source of genetic and phenotypic diversity. It suggests that the copy number variation of function gene maybe leads to the phenotypic changes. Kupple like factor 3 (KLF3) gene is a vital transcription factor associated with the growth and development of muscle and adipose tissue. It has been mapped in a CNV region by animal genome re-sequencing. In this study, we detected the distribution diversity of KLF3 gene copy numbers in six Chinese cattle breeds (QC, NY, XN, PN, QDM and JX) and associated the phenotypic traits with it. Then, we analyzed the KLF3 gene transcription expression level in different tissues of Jiaxian (JX) cattle. Furthermore, we detected mRNA expression level of muscle and fat tissues of Jiaxian cattle (JX), Angus × Jiaxian (AJ). The results showed that the copy number in CNV loss was more frequent in QC than others. And we revealed a positive effect of KLF3 CNV on growth traits, such as body mass and heart girth (P < 0.05). In a word, we ascertained the significance between CNVs of KLF3 gene and growth traits in different cattle breeds, and our data indicates that the CNVs of KLF3 gene may as a marker for the future molecular breeding of Chinese beef cattle.


Assuntos
Tecido Adiposo/crescimento & desenvolvimento , Variações do Número de Cópias de DNA , Estudos de Associação Genética/métodos , Fatores de Transcrição Kruppel-Like/genética , Músculo Esquelético/crescimento & desenvolvimento , Animais , Peso Corporal , Bovinos , Mapeamento Cromossômico , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Fenótipo , Característica Quantitativa Herdável , Análise de Sequência de DNA
6.
Anim Biotechnol ; 30(1): 30-35, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29540101

RESUMO

As a member of MYLK family, MYLK4 gene may play a vital role in muscle development. In this study, one novel single-nucleotide polymorphism (SNP) was identified the bovine MYLK4 by sequencing pooled DNA samples (pool-Seq) and forced polymerase chain reaction-restriction fragment length polymorphism (forced PCR-RFLP) methods. Overall, we reported one mutation (SNP1) in the intron 10 region within the bovine MYLK4 gene in 559 individuals representing five main cattle breeds from China (Nanyang, NY; Qinchuan; Jiaxian, JX; Pinan cattle; and Caidamu cattle, CDM). Genotype AA and allele A were predominant in the QC, PN, and XN populations. Association analysis with growth traits in the QC breed showed that the animals with genotype GG had significantly greater chest breadth and hip width (P < 0.05). Meanwhile, the genotype GG was strongly associated with withers height and body length than those with genotype AA (P < 0.01 or P < 0.05) at 12 months in the NY breed. These statistical results exhibited that the MYLK4 gene might be a potential candidate gene to improve cattle's growth traits, and the SNP could be used as molecular markers in early marker-assisted selection (MAS) in beef cattle breeding program.


Assuntos
Bovinos/genética , Polimorfismo de Nucleotídeo Único/genética , Alelos , Animais , Cruzamento , Bovinos/anatomia & histologia , Bovinos/crescimento & desenvolvimento , Feminino , Estudos de Associação Genética/veterinária , Marcadores Genéticos/genética , Variação Genética , Genótipo , Fenótipo , Reação em Cadeia da Polimerase/veterinária , Polimorfismo de Fragmento de Restrição , Análise de Sequência de DNA/veterinária
7.
Gene ; 689: 166-171, 2019 Mar 20.
Artigo em Inglês | MEDLINE | ID: mdl-30580072

RESUMO

Genetic polymorphism has great influences on the improvement of cattle traits. The polymorphism of the same gene family will greatly change the growth traits of cattle, such as the pleomorphic adenoma gene (PLAG) family. Many studies have shown that the PLAG family proteins are the transcription regulators of nuclear protein, which mainly regulates the expression of many important genes in the body. In cattle, single nucleotide polymorphisms (SNPs) within or near the PLAG1 gene is associated with economic traits of height in cattle. Here we investigate a SNPs of bovine PLAG1 in 646 cattle from five breeds. We found three different genotypes by using cleaved amplification polymorphism sequence-tagged sites (CAPs), includes some significant differences in body height, chest circumference and other shapes (P < 0.05), also we found that the TT genotype had no advantage in body shape. These results indicate that the selection of PLAG1 gene could be used to ensure the breeding direction for growth traits of the beef cattle.


Assuntos
Bovinos/crescimento & desenvolvimento , Bovinos/genética , Proteínas de Ligação a DNA/genética , Polimorfismo de Nucleotídeo Único , Animais , Tamanho Corporal/genética , Peso Corporal/genética , Cruzamento , China , Genótipo , Fenótipo , Característica Quantitativa Herdável
8.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-269226

RESUMO

Objective To evaluate the health related quality of life (HRQoL) and to explore the influencing factors related to the prevalence of the essential hypertension,diabetes,coronary heart disease (CHD) and stroke in middle-aged and elderly people from rural communities.Methods A total of 5345 individuals were chosen from a 2010 Health Survey in Fangshan,Beijing.Self-designed questionnaire was applied to collect the information on general health-related behaviors,chronic conditions,self-rated health,blood pressure and HRQoL with the EuroQoL questionnaire (EQ-5D) were measured.Probit regression model was used to identify the influencing factors on HRQoL,adjusting age,marriage status,education level,smoking,alcohol intake,physical activity and control of blood pressure.Population Attributable Risk Proportion (PARP) for estimating the influence of chronic disease on HRQoL was also calculated.Results The average EQ-5D index was 0.923 ±0.145,with 72.1% of the overall respondents in the status of having chronic diseases.Participants with chronic diseases had significantly lower EQ-5D index (0.907 ± 0.155 ) than those without (0.963 ±0.105 ) (t =15.082,P< 0.001 ).Significant relations were found between a lower HRQoL and chronic diseases.Relative risk (RR) and 95% confidence interval (95% CI) of poor HRQoL in populations with hypertension,diabetes,CHD and stroke were 1.686 (95%CI: 1.519-1.871),1.725 (95%CI:1.502-1.981 ),1.869 (95%CI: 1.663-2.099),and 1.759 (95%CI: 1.474-2.089) respectively.The most influential disease appeared to be stroke in male (RR=1.929,95%CI: 1.462-2.546),whereas CHD in female individuals (RR=1.926,95%CI: 1.671-2.220).Rates of PARP (PAR%) for poor HRQoL in chronic disease subgroups were as follow: hypertension 31.05%,CHD 23.39%,diabetes 4.84% and stroke 4.44%,respectively.Conclusion This study suggested that stroke,at individual level,was the major influential factor to HRQoL.However,hypertension remained the leading preventable influential factor to HRQoL at the population level.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...