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1.
Arq. bras. med. vet. zootec ; 65(6): 1609-1615, Dec. 2013. tab
Article in Portuguese | LILACS | ID: lil-696838

ABSTRACT

O objetivo deste estudo foi buscar associação entre a taxa de prenhez após inseminação e natalidade com marcadores moleculares ligados aos genes do receptor para IGF-1, LHβ, Leptina e receptores do FSH e LH. Utilizaram-se 249 vacas adultas Aberdeen Angus, das quais 199 foram submetidas a protocolos distintos para a IATF, seguida pelo repasse com touros, e 50 vacas formaram o grupo controle representado pelo acasalamento com touros. Foram avaliados o escore de condição corporal (ECC) e o escore de condição ovariana (ECO) ao início da estação reprodutiva. O ECC influenciou a taxa de natalidade, respectivamente de 55,6%, 75,8% e 82,4% (P<0,05) para os animais com ECC menor que 2,5, entre 2,5 a 2,9, e maior ou igual a 3,0, por ocasião da estação reprodutiva. Os marcadores relacionados ao gene do receptor para o IGF-1 (AFZ-1 e HEL5) mostraram associação com a taxa de natalidade. Vacas homozigóticas para o marcador AFZ-1 apresentaram 84,4% de natalidade em comparação às heterozigóticas, com 71,5% (P<0,05). A presença do alelo*161 para o marcador HEL5 foi negativa sobre a natalidade, respectivamente de 33,3% e 76,5% para vacas com e sem esse alelo (P<0,05). Esses resultados demonstram uma importante associação entre os marcadores envolvidos com o receptor para o IGF-1 e desempenho reprodutivo de vacas Angus.


The association between the reproductive performance, expressed by pregnancy rate at fixed timed artificial insemination and birth rate in the subsequent season in beef cows, and molecular markers linked to genes for IGF-1 receptor, LHβ, leptin, and FSH and LH receptors were evaluated. Data from 249 Aberdeen Angus adult cows were used in this study. One hundred and ninety-nine cows were subjected to four different protocols for FTAI, followed by clean-up bulls and 50 cows formed the control group, matted only with bulls for 90 days during the mating season. Body condition score (BCS) and ovarian condition score (OCE) were evaluated at the beginning of the breeding season. The birth rate in the following year was 75.5%, with no treatments influence. The BCS has influenced the birth rate, respectively 55.6%, 75.8% and 82.4% (P<0.05) for animals with BCS less than 2.5; 2.5 to 2.9; and greater than or equal to 3.0, at the beginning of the breeding season. The markers related to IGF-1 receptor gene (AFZ-1 and HEL5) were associated with the birth rate in beef cows. Cows homozygous for AFZ-1 marker showed 84.4% of birth rate, while heterozygous cows showed 71.5% (P <0.05). The presence of allele *161 to the HEL5 marker was negative on birth rate. Cows with this allele had only 33.3% of birth rate, while cows without this allele had 76.5% of birth rate (P <0.05). These results demonstrate a significant association between the markers involved with the IGF-1 receptor and reproductive performance of Aberdeen Angus beef cows.


Subject(s)
Animals , Cattle , Birth Rate , Insulin-Like Growth Factor I/analysis , Fertility/physiology , Cattle
2.
Genet. mol. biol ; 22(2): 151-61, jun. 1999. ilus, mapas, tab
Article in English | LILACS | ID: lil-242193

ABSTRACT

A total of 2,708 individuals from the European-derived population of Rio Grande do Sul, divided into seven mesoregions, and of 226 individuals of similar origin from Santa Catarina were studied. Seventeen protein genetic systems, as well as grandparents' nationalities, individuals' surnames, and interethnic admixture were investigated. The alleles which presented the highest and lowest differences were GLO1*2 (16 per cent) and PGD*A (2 per cent), respectively, but in general no significant genetic differences were found among mesoregions. The values observed were generally those expected for individuals of European descent, with the largest difference being a lower prevalence (34-39per cent) of P*1. Significant heterogeneity among mesoregions was observed for the other variables considered, and was consistent with historical records. The Amerindian contribution to the gene pool of European-derived subjects in Rio Grande do Sul was estimated to be as high as 11 per cent. Based on the four data sets, the most general finding was a tendency for a northeast-southwest separation of the populations studied. Seven significant phenotype associations between systems were observed at the 5 per cent level (three at the 0.1 per cent level). Of the latter, the two most interesting (since they were also observed in other studies) were MNSs/Duffy and Rh/ACP.


Subject(s)
Humans , Alleles , Genetic Variation , Ethnicity/genetics , Haplotypes , Pedigree , Proteins/genetics , Brazil/ethnology , Europe , Multivariate Analysis , Phenotype
3.
Indian J Hum Genet ; 1995 Apr; 1(2): 105-110
Article in English | IMSEAR | ID: sea-159772

ABSTRACT

A review is made of 961 cases of paternity determinations using a battery of 18 protein genetic systems. With this set, the a priori probability of exclusion is 89% but only 16% of the accused men were exonerated. Among the non-excluded, 55% had probabilities of 95% or more of being the father of the child considered. The results are in accordance with those from other centers which use equivalent sets of protein markers. When the direct study of DNA is not possible, these tests provide a relatively low-cost, reliable alternative for such determinations.

4.
Rev. bras. genét ; 11(4): 949-55, Dec. 1988. tab
Article in English | LILACS | ID: lil-62629

ABSTRACT

A fosfoglucomutase placental (locos PGM1, PGM2 e PGN3) foi investigada em uma amostra de 442 recém-nascidos (54% Brancos e 46% Negros) da populaçäo de Porto Alegre. As freqüências gênicas observadas foram: Branco: PGMI*2 = 0.24, PGM2*1 = 1.00 e PGm3*2 = 0.32; Negros: PGM1*2 = 0.22, PGM2*1 = 1.00 e PGM3*2 = 0.45. Detectou-se entre os negros um indivíduo heterozigoto para um possível alelo nulo no loco PGM1. Näo foi verificada associaçäo nas distribuiçöes conjuntas entre os locos PGN1 e PGM3, bem como, näo se encontrou efeito dos fenótipos de PGN1 e PGM3 no desenvolvimento do feto ou da placenta


Subject(s)
Infant, Newborn , Humans , Gene Frequency , Phosphoglucomutase/analysis , Placenta/enzymology , Polymorphism, Genetic , Brazil , Phenotype
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