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1.
Theriogenology ; 128: 47-53, 2019 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-30743103

RESUMEN

This study estimated the genetic variability and correlations between growth and reproductive traits in Nelore cattle. Annual genetic changes in female reproductive traits were also evaluated using repeated measures. Direct heritability was moderate for the growth traits and scrotal circumference (0.235 ±â€¯0.015 to 0.443 ±â€¯0.006), indicating genetic variability in these traits in the population studied. Maternal heritability was low for weaning height (0.042 ±â€¯0.012) and weaning weight (0.112 ±â€¯0.013). Regarding female reproductive traits, gestation length (GL) exhibited a slightly higher heritability (0.179 ±â€¯0.006) than days to calving (DC) and calving interval (CI) (0.123 ±â€¯0.006 and 0.105 ±â€¯0.008, respectively). Repeatability was lower for GL (0.222 ±â€¯0.006) compared to DC (0.318 ±â€¯0.004) and CI (0.406 ±â€¯0.006). Moderate and positive genetic correlations were obtained between the growth traits and scrotal circumference, ranging from 0.193 ±â€¯0.019 to 0.519 ±â€¯0.007. Weaning height showed low and positive genetic associations with GL (0.138 ±â€¯0.007) and CI (0.189 ±â€¯0.016), but was not correlated with DC (-0.016 ±â€¯0.011). Similarly, weaning weight, yearling height or yearling weight was not associated with any of the female reproductive traits. The genetic correlations between scrotal circumference and female reproductive traits were negative and favorable, but low: -0.116 ±â€¯0.020 (GL), -0.084 ±â€¯0.028 (DC), and -0.054 ±â€¯0.038 (CI). Favorable genetic associations were estimated between all female reproductive traits, ranging from 0.170 ±â€¯0.040 to 0.442 ±â€¯0.050. Genetic changes were favorable for GL and CI (-0.02 days/year and -0.11 days/year, respectively) and unfavorable for DC (0.16 days/year). In conclusion, selection for higher growth using the estimated breeding values for height and weight will not affect the reproductive performance of Nelore females. Nonetheless, simultaneous selection for growth and reproductive traits is possible.


Asunto(s)
Bovinos/fisiología , Reproducción/genética , Escroto/anatomía & histología , Animales , Teorema de Bayes , Cruzamiento , Bovinos/anatomía & histología , Bovinos/crecimiento & desarrollo , Femenino , Masculino , Destete
2.
Theriogenology ; 118: 27-33, 2018 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-29883841

RESUMEN

The size and body condition of cows can affect their reproductive efficiency. However, few studies reported genetic correlations between these traits in beef cattle. Thus, we estimated the genetic parameters and correlations between weight (MW), height (MH) and body condition score (BCS) of cows and reproductive traits (SC: scrotal circumference, AFC: age at first calving, GL: gestation length, DC: days to calving, and CI: calving interval) in Nelore animals. In addition, it has also obtained direct and correlated responses aiming at determining whether changes in cow size and body condition may affect the herd reproductive performance. A series of two-trait Bayesian analyzes were performed including MW, MH or BCS with each of the reproductive traits. The heritability estimated for MW, MH and BCS were 0.46 ±â€¯0.02, 0.35 ±â€¯0.01 and 0.17 ±â€¯0.02, indicating an involvement of additive gene action mainly in cows' size determination. For the reproductive traits of females, heritability ranged from 0.05 ±â€¯0.00 for CI to 0.18 ±â€¯0.01 for GL, and was 0.37 ±â€¯0.01 for SC. Low repeatability were estimates for GL (0.19 ±â€¯0.00), DC (0.19 ±â€¯0.00) and CI (0.05 ±â€¯0.00). The MW was positive correlated with AFC (0.23 ±â€¯0.08), CI (0.25 ±â€¯0.15) and, with lower magnitude, of GL (0.14 ±â€¯0.03). Null genetic correlations were obtained between MW with SC (0.03 ±â€¯0.03) and DC (-0.01 ±â€¯0.04). The MH showed positive and low genetic association with all female reproductive traits, but negative with SC (-0.08 ±â€¯0.03). Negative and favorable genetic correlations were estimated between BCS and females reproductive traits, but unfavorable with SC (-0.13 ±â€¯0.06). In summary, the negative impact of increase the size of Nelore females on their reproductive performance is expected to be small in tropical regions. The use of sires with high genetic breeding values for SC should result in slight reduction of BCS of cows, but no effective genetic response in female size is expected. Selection based on BCS should promote little improvement in reproductive efficiency of cows.


Asunto(s)
Composición Corporal/fisiología , Tamaño Corporal/fisiología , Bovinos/genética , Reproducción/genética , Reproducción/fisiología , Animales , Estatura/genética , Peso Corporal/genética , Cruzamiento , Bovinos/fisiología , Femenino , Edad Gestacional , Humanos , Masculino , Carácter Cuantitativo Heredable , Escroto/anatomía & histología
3.
Theriogenology ; 108: 81-87, 2018 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-29197296

RESUMEN

The female reproductive performance, productivity and size are strongly associated with production efficiency of herds raised in a tropical environment. The age at first calving (AFC), accumulated productivity (AP), stayability (STAY) and mature weight (MW) could be used as indicators of these traits. In this study, the genetic parameters and correlations between AFC, AP, STAY and MW measured in Nellore females were estimated, in order to provide support for the beef cattle evaluation programs. In addition, the genetic changes for these traits were obtained. The (co)variance components were estimated by Gibbs sampling by four-trait multivariate analysis, using a threshold animal model for STAY and linear animal model for the other traits (AFC, AP and MW). Heritability of AFC, AP and STAY showed low values, with posterior means of 0.13 ± 0.02, 0.14 ± 0.01 and 0.19 ± 0.03, respectively. On the other hand, for MW were estimated mean heritability of 0.44 ± 0.03 and repeatability of 0.77 ± 0.03, demonstrating the importance of genetic and permanent environmental effects for the expression of beef cows' size. The AFC showed null genetic correlation with AP (-0.06 ± 0.12) and MW (0.01 ± 0.09) and low and negative with STAY (-0.15 ± 0.11). The AP showed high genetic correlation with STAY (0.86 ± 0.03) and weak with MW (0.23 ± 0.09). Positive and moderate genetic association was estimated between STAY and MW (0.66 ± 0.05). Annual direct genetic trends of 0.19 kg, 0.30 units and 0.10 kg were estimated for AP, STAY and MW, respectively, and were significant (P < 0.05) for STAY and MW. For AFC, negative and favorable annual genetic change was estimated (-0.08 months, P < 0.05). In this population, the selection of heifers for an early reproductive age should have little influence, however favorable, in the time that the cows remain in the herd. The use of AP as a selection criterion should result in smaller changes in the females' mature weight when compared to selection based on STAY.


Asunto(s)
Peso Corporal/genética , Bovinos/genética , Fertilidad/genética , Reproducción/genética , Animales , Femenino , Modelos Genéticos , Carácter Cuantitativo Heredable
4.
Genet Mol Res ; 16(1)2017 Mar 22.
Artículo en Inglés | MEDLINE | ID: mdl-28340271

RESUMEN

Fertility traits, such as heifer pregnancy, are economically important in cattle production systems, and are therefore, used in genetic selection programs. The aim of this study was to identify single nucleotide polymorphisms (SNPs) using RNA-sequencing (RNA-Seq) data from ovary, uterus, endometrium, pituitary gland, hypothalamus, liver, longissimus dorsi muscle, and adipose tissue in 62 candidate genes associated with heifer puberty in cattle. RNA-Seq reads were assembled to the bovine reference genome (UMD 3.1.1) and analyzed in five cattle breeds; Brangus, Brahman, Nellore, Angus, and Holstein. Two approaches used the Brangus data for SNP discovery 1) pooling all samples, and 2) within each individual sample. These approaches revealed 1157 SNPs. These were compared with those identified in the pooled samples of the other breeds. Overall, 172 SNPs within 13 genes (CPNE5, FAM19A4, FOXN4, KLF1, LOC777593, MGC157266, NEBL, NRXN3, PEPT-1, PPP3CA, SCG5, TSG101, and TSHR) were concordant in the five breeds. Using Ensembl's Variant Effector Predictor, we determined that 12% of SNPs were in exons (71% synonymous, 29% nonsynonymous), 1% were in untranslated regions (UTRs), 86% were in introns, and 1% were in intergenic regions. Since these SNPs were discovered in RNA, the variants were predicted to be within exons or UTRs. Overall, 160 novel transcripts in 42 candidate genes and five novel genes overlapping five candidate genes were observed. In conclusion, 1157 SNPs were identified in 62 candidate genes associated with puberty in Brangus cattle, of which, 172 were concordant in the five cattle breeds. Novel transcripts and genes were also identified.


Asunto(s)
Pubertad/genética , Animales , Secuencia de Bases , Bovinos , Femenino , Fertilidad/genética , Genoma , Masculino , Polimorfismo de Nucleótido Simple , Embarazo , ARN/genética , Selección Genética , Análisis de Secuencia de ARN/métodos , Maduración Sexual
5.
Trop Anim Health Prod ; 48(8): 1679-1684, 2016 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-27627906

RESUMEN

Estimation and prediction ability of linear and threshold models for yearling breed quality score (BQ) and navel development score at weaning (WN) and yearling (YN), considering variances, heritabilities, and rank correlations based on the breeding values predicted for bulls, were compared. Furthermore, it was determined whether BQ, WN, and YN are genetically associated with growth traits (BWG: birth to weaning weight gain, WH: weaning height, WYG: weaning to yearling weight gain, YH: yearling height) to field data of Nelore cattle. For BQ, similar heritabilities were estimated using linear (0.14 ± 0.01) and threshold (0.15 ± 0.02) models. For navel development scores, higher heritability was estimated with threshold (WN 0.22 ± 0.03; YN 0.42 ± 0.03) rather than linear (WN 0.16 ± 0.01; YN 0.29 ± 0.01) models. Rank correlations between sires breeding values predicted for visual scores with linear and threshold models ranging from 0.53 to 0.98, indicating that different sires would be selected using these models, mainly for higher selection intensities. The BQ showed little genetic variability and was not associated with WH and YH. However, low and positive genetic correlations were obtained between BQ with BWG (0.27 ± 0.02) and WYG (0.25 ± 0.02). In general, they are expected low genetic gains for BQ as correlated response to selection based on any of the growth traits studied. The WN showed higher genetic correlation with BWG (0.63 ± 0.02) and WH (0.53 ± 0.02) rather than WYG (-0.06 ± 0.02) and YH (0.26 ± 0.02), indicating that selection for increased growth at weaning (height and weight gain) should lead to longer and most pendulous navels at this age. Weak genetic correlations were obtained between yearling navel and growth traits.


Asunto(s)
Bovinos/fisiología , Modelos Genéticos , Carne Roja , Aumento de Peso , Animales , Cruzamiento , Bovinos/crecimiento & desarrollo , Femenino , Masculino , Fenotipo , Destete
6.
J Anim Sci ; 94(12): 5014-5022, 2016 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28046186

RESUMEN

Principal component analysis was applied to evaluate the variability and relationships among univariate breeding values predicted for 9 weaning and yearling traits, as well as suggest functions of the traits that would promote a particular breeding objective. Phenotypic and pedigree information from 600,132 Nelore animals was used. Genetic parameters and breeding values were obtained from univariate analyses of birth to weaning weight gain; weaning to yearling weight gain; conformation, finishing precocity, and muscling scores at weaning and at yearling; and yearling scrotal circumference. The principal component mainly associated with maturity (precocious vs. late animals) was used as a pseudophenotype in bivariate analyses with either adult weight or adult height of cows. Direct heritability estimates ranging from 0.19 ± 0.01 to 0.41 ± 0.01 indicate that these 9 traits are all heritable to varying degrees. Correlations between the breeding values for the various traits ranged from 0.14 to 0.88. Principal component analysis was performed on the standardized breeding values. The first 3 principal components attained the Kaiser criterion, retaining 48.06%, 18.03%, and 12.97% of the total breeding value variance, respectively. The first component was characterized by positive coefficients for all traits. The second component contrasted weaning traits with yearling traits. The third component represented a contrast between late maturity animals (better for weight gain and conformation) and early maturity animals (better for finishing precocity, muscling, and scrotal circumference). Thus, the first 3 components represent 3 different potential selection criteria. Selecting for the first principal component would identify animals with positive breeding values for all studied traits. The second principal component may be used to identify animals with higher or lower maturation rates (precocity). Animals with negative values in the third principal component are regarded as early maturing. Genetic correlations between maturity (third principal component) with adult weight and adult height were 0.19 ± 0.02 and 0.32 ± 0.02, respectively. These results showed that the weaning and yearling bovine maturity is genetically associated with the adult size of the cows used in reproduction.


Asunto(s)
Bovinos/fisiología , Modelos Estadísticos , Reproducción , Animales , Peso Corporal , Cruzamiento , Bovinos/genética , Bovinos/crecimiento & desarrollo , Femenino , Masculino , Linaje , Fenotipo , Análisis de Componente Principal , Carne Roja , Escroto , Destete , Aumento de Peso
7.
Genet Mol Res ; 14(3): 11133-44, 2015 Sep 22.
Artículo en Inglés | MEDLINE | ID: mdl-26400344

RESUMEN

The objective of this study was to evaluate associations between single nucleotide polymorphism (SNP) markers and carcass traits measured postmortem in Nellore cattle. Records of loin eye area (LEA) and backfat thickness (BF) from 740 males and records of hot carcass weight (HCW) from 726 males were analyzed. All of the animals were genotyped using the BovineHD BeadChip. Association analyses were performed by the restricted maximum likelihood method that considered one SNP at a time. Significant SNPs were identified on chromosomes 2 and 6 for LEA and on chromosomes 7, 1, and 2 for BF. For HCW, associations with SNPs were found on chromosomes 13, 14, and 28, in addition to genome regions that were directly related to this trait, such as the EFCAB8 and VSTM2L genes, and to bone development (RHOU). Some SNPs were located in very close proximity to genes involved in basal metabolism (BLCAP, NNAT, CTNNBL1, TGM2, and LOC100296770) and the immune system (BPI).


Asunto(s)
Carne/normas , Animales , Peso Corporal/genética , Bovinos/genética , Bovinos/crecimiento & desarrollo , Calidad de los Alimentos , Frecuencia de los Genes , Marcadores Genéticos , Estudio de Asociación del Genoma Completo , Genotipo , Masculino , Músculo Esquelético/fisiología , Polimorfismo de Nucleótido Simple , Grasa Subcutánea/anatomía & histología
8.
Genet Mol Res ; 14(1): 234-43, 2015 Jan 16.
Artículo en Inglés | MEDLINE | ID: mdl-25729955

RESUMEN

The objective of this study was to identify associations between known polymorphisms in genes related to adipose tissue and sexual precocity in Nellore cattle. A total of 1689 precocious and non-precocious heifers belonging to farms participating in Conexão Delta G breeding program were studied. SNPs from the Illumina High-Density Bovine SNP BeadChip were used. This chip contains 777,000 SNPs located within the region of the candidate genes at a distance of up to 5 kb, considering that linkage disequilibrium (LD) exists at this distance. Linear models were used for statistical analysis. The fastPHASE and GenomeStudio programs were used for haplotype reconstruction and LD analysis based on r2 statistics. Fifty-seven candidate genes and 443 SNPs were analyzed: among the latter, 370 SNPs formed 83 haplotypes, while the remaining SNPs were studied separately. Statistical analysis showed that only three haplotypes, one haplotype consisting of two SNPs located in the FABP4 gene and two haplotypes consisting of four and two SNPs located in the PPP3CA gene, had a significant effect on sexual precocity at P < 0.05. It can be concluded that the FABP4 and PPP3CA genes influence sexual precocity and may therefore be used in selection programs designed to improve sexual precocity in Nellore cattle.


Asunto(s)
Bovinos/genética , Estudios de Asociación Genética , Metabolismo de los Lípidos/genética , Pubertad Precoz/genética , Animales , Cromosomas de los Mamíferos/genética , ADN/aislamiento & purificación , Femenino , Frecuencia de los Genes , Técnicas de Genotipaje , Haplotipos , Masculino , Polimorfismo de Nucleótido Simple
9.
Theriogenology ; 83(8): 1338-43, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25726150

RESUMEN

In beef cattle genetic evaluation, principal component models of the additive genetic effect could be used to incorporate several traits in the same analysis, without an important increase in the number of parameters to be estimated. In this study, multitrait (MT) and reduced-rank models were compared for their ability to estimate parameters and predict breeding values for weaning weight, yearling weight, weaning hip height, yearling hip height, weaning to yearling weight gain, scrotal circumference, and age at the first calving. Data obtained were from 74,388 Nelore animals, born to 1441 sires and 28,502 cows. Six analyses were performed using a MT model that incorporated all the traits simultaneously and five reduced-rank models for the genetic additive direct (co)variance matrix, fitting the first one (PC1), two (PC2), three (PC3), four (PC4), and five (PC5) principal components. The model considering the first three principal components (PC3) provided the best fit. Direct and maternal heritability and the respective standard errors obtained from the MT and PC3 models were similar. In general, the PC3 model provided slightly stronger genetic correlations between the traits when compared with those obtained with the MT model. The rank correlations between the breeding values predicted with the MT and PC3 models for the different traits ranged from 0.93 to 0.99. When 2% and 10% of the best sires were selected on the basis of breeding values predicted by the MT model, the degree of concordance with the PC3 model ranged from 86% to 97%. The first three principal components explained most of the genetic variation among animals, suggesting that major changes should not be expected in the sire's classification on the basis of breeding values predicted for growth and reproductive traits. Models of principal components could be used for beef cattle genetic evaluation, especially when considering several economic traits in the same analysis.


Asunto(s)
Bovinos/genética , Carácter Cuantitativo Heredable , Reproducción/genética , Aumento de Peso/genética , Factores de Edad , Animales , Peso Corporal/genética , Cruzamiento , Bovinos/fisiología , Femenino , Masculino , Modelos Genéticos , Análisis de Componente Principal , Escroto/crecimiento & desarrollo , Destete
10.
Genet Mol Res ; 9(4): 2050-9, 2010 Oct 19.
Artículo en Inglés | MEDLINE | ID: mdl-20967695

RESUMEN

We analyzed the polymorphisms TFAM HaeIII, TFAM MboI and FABP4 MspA1I in three Nellore lines selected for growth in order to evaluate how selection affects the frequencies of these polymorphisms and evaluate their association with growth and carcass traits in Zebu cattle. Birth, weaning and yearling weights, rump height, longissimus muscle area, backfat thickness, and rump fat thickness were analyzed. The sample was constituted of animals from two lines selected for yearling weight (NeS and NeT), and a control line (NeC), established in 1980, at the São Paulo Instituto de Zootecnia. Two hundred and seventy-two heifers were genotyped for TFAM gene SNPs, and 325 heifers were genotyped for the FABP4 SNP. High frequencies were observed for the alleles A (TFAM HaeIII), C (TFAM MboI) and C (FABP4 MspA1I). Significant differences in allele frequencies between NeS and NeT were observed for the TFAM HaeIII, and between the line NeT and lines NeC and NeS for the FABP4 MspA1I SNP. Five haplotypes were observed for the two polymorphisms in the TFAM gene, haplotype AACC being the most frequent. None of the markers separately or according to haplotype was significantly associated with the growth and carcass traits. The low frequencies of alleles that are associated with high marbling scores and thick subcutaneous fat in taurine breeds might explain the low means for these traits in Nellore cattle.


Asunto(s)
Bovinos/genética , Proteínas de Unión a Ácidos Grasos/genética , Polimorfismo Genético , Factores de Transcripción/genética , Animales , Bovinos/crecimiento & desarrollo
11.
J Anim Sci ; 88(2): 435-41, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19820053

RESUMEN

The aim of this study was to analyze LEP and DGAT1 gene polymorphisms in 3 Nelore lines selected for growth and to evaluate their effects on growth and carcass traits. Traits analyzed were birth, weaning, and yearling weight, rump height, LM area, backfat thickness, and rump fat thickness obtained by ultrasound. Two SNP in the LEP gene [LEP 1620(A/G) and LEP 305(T/C)] and the K232A mutation in the DGAT1 gene were analyzed. The sample consisted of 357 Nelore heifers from 2 lines selected for yearling weight and a control line, established in 1980, at the Estação Experimental de Zootecnia de Sertãozinho (Sertãozinho, Brazil). Three genotypes were obtained for each marker. Differences in allele frequencies among the 3 lines were only observed for the DGAT1 K232A polymorphism, with the frequency of the A allele being greater in the control line than in the selected lines. The DGAT1 K232A mutation was associated only with rump height, whereas LEP 1620(A/G) was associated with weaning weight and LEP 305(T/C) with birth weight and backfat thickness. However, more studies, with larger data sets, are necessary before these makers can be used for marker-assisted selection.


Asunto(s)
Bovinos/genética , Diacilglicerol O-Acetiltransferasa/genética , Leptina/genética , Polimorfismo de Nucleótido Simple/genética , Alelos , Animales , Bovinos/crecimiento & desarrollo , Femenino , Frecuencia de los Genes/genética , Marcadores Genéticos/genética , Genotipo , Masculino , Carne/normas , Músculo Esquelético/crecimiento & desarrollo , Reacción en Cadena de la Polimerasa , Sitios de Carácter Cuantitativo/genética , Análisis de Secuencia de ADN , Homología de Secuencia de Ácido Nucleico
12.
Braz J Med Biol Res ; 40(6): 793-7, 2007 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17581677

RESUMEN

Pregnancy loss can be caused by several factors involved in human reproduction. Although up to 50% of cases remain unexplained, it has been postulated that the major cause of failed pregnancy is an error of embryo implantation. Transmembrane mucin-1 (MUC-1) is a glycoprotein expressed on the endometrial cell surface which acts as a barrier to implantation. The gene that codes for this molecule is composed of a polymorphic tandem repeat of 60 nucleotides. Our objective was to determine if MUC-1 genetic polymorphism is associated with implantation failure in patients with a history of recurrent abortion. The study was conducted on 10 women aged 25 to 35 years with no history of successful pregnancy and with a diagnosis of infertility. The control group consisted of 32 patients aged 25 to 35 years who had delivered at least two full-term live children and who had no history of abortions or fetal losses. MUC-1 amplicons were obtained by PCR and observed on agarose and polyacrylamide gel after electrophoresis. Statistical analysis showed no significant difference in the number of MUC-1 variable number of tandem repeats between these groups (P > 0.05). Our results suggest that there is no effect of the polymorphic MUC-1 sequence on the implantation failure. However, the data do not exclude MUC-1 relevance during embryo implantation. The process is related to several associated factors such as the mechanisms of gene expression in the uterus, specific MUC-1 post-translational modifications and appropriate interactions with other molecules during embryo implantation.


Asunto(s)
Aborto Habitual/genética , Implantación del Embrión/genética , Infertilidad Femenina/genética , Mucina-1/genética , Polimorfismo Genético , Adulto , Estudios de Casos y Controles , Electroforesis en Gel de Poliacrilamida , Femenino , Humanos , Reacción en Cadena de la Polimerasa , Embarazo
13.
Braz. j. med. biol. res ; 40(6): 793-797, June 2007. ilus
Artículo en Inglés | LILACS | ID: lil-452679

RESUMEN

Pregnancy loss can be caused by several factors involved in human reproduction. Although up to 50 percent of cases remain unexplained, it has been postulated that the major cause of failed pregnancy is an error of embryo implantation. Transmembrane mucin-1 (MUC-1) is a glycoprotein expressed on the endometrial cell surface which acts as a barrier to implantation. The gene that codes for this molecule is composed of a polymorphic tandem repeat of 60 nucleotides. Our objective was to determine if MUC-1 genetic polymorphism is associated with implantation failure in patients with a history of recurrent abortion. The study was conducted on 10 women aged 25 to 35 years with no history of successful pregnancy and with a diagnosis of infertility. The control group consisted of 32 patients aged 25 to 35 years who had delivered at least two full-term live children and who had no history of abortions or fetal losses. MUC-1 amplicons were obtained by PCR and observed on agarose and polyacrylamide gel after electrophoresis. Statistical analysis showed no significant difference in the number of MUC-1 variable number of tandem repeats between these groups (P > 0.05). Our results suggest that there is no effect of the polymorphic MUC-1 sequence on the implantation failure. However, the data do not exclude MUC-1 relevance during embryo implantation. The process is related to several associated factors such as the mechanisms of gene expression in the uterus, specific MUC-1 post-translational modifications and appropriate interactions with other molecules during embryo implantation.


Asunto(s)
Adulto , Femenino , Humanos , Embarazo , Aborto Habitual/genética , /genética , Implantación del Embrión/genética , Infertilidad Femenina/genética , Polimorfismo Genético , Estudios de Casos y Controles , Electroforesis en Gel de Poliacrilamida , Reacción en Cadena de la Polimerasa
14.
J Anim Breed Genet ; 124(1): 42-6, 2007 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-17302961

RESUMEN

MUC1 is a transmembrane glycoprotein expressed on the apical surfaces of the uterine epithelial tissue with predicted functions in protection and cell-cell adhesion. These properties are closely related with the repetitive region [variable number of tandem repeats (VNTR)] of the extracellullar domain and with the O-glycosylation in their serine and threonine residues. This study describes a polymerase chain reaction (PCR) protocol to analyse MUC1 bovine genetic polymorphism and demonstrates the existence of a VNTR within the sites for O-glycosylation. Oligonucleotide primers based on the Bos taurus mucin (MUC1) gene sequence GenBank AF399757 were used to amplify five VNTR MUC1 alleles from a study group of 56 pure Nelore bovines. The number of repeats varied between 10 and 24, being more prevalent than the alleles with less number of repeats. The DNA sequence analysis revealed two repeats and one of them presented 100% homology with the bovine consensus sequence already reported. The second repeat showed codons that translate to serine and proline amino acids, which are conserved in the MUC1 of several species. This study is the first description of allelic variation and the VNTR structure in the Nelore breed MUC1 gene, and we suggest that this genetic variability can be tested for association with variation in reproductive traits in Nelore cattle.


Asunto(s)
Bovinos/genética , Mucina-1/genética , Polimorfismo Genético , Animales , Secuencia de Bases , Cartilla de ADN , Frecuencia de los Genes , Repeticiones de Minisatélite/genética , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Análisis de Secuencia de ADN , Homología de Secuencia
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