A raça Gir Mocha na região Nordeste do Brasil: estrutura genética populacional via análise de pedigree / The Polled Gir Polled in Northeastern Brazil: population genetic structure via analysis of pedigree

Foram utilizados dados de pedigree de 2.558 bovinos da raça Gir Mocha nascidos no período de 1954 a 2005. As análises foram realizadas utilizando-se o programa Endog. Do total de animais estudados, 61,9%; 10,6% e 0,1% possuíam pedigree na primeira, segunda e terceira gerações, respectivamente.O número efetivo de rebanhos que forneceram machos reprodutores foi de 10,25 para pais e 3,87 para avôs, confirmando a baixa integralidade do pedigree. O número de animais fundadores foi de 975,5, e o número efetivo de fundadores de 141,34. O número de ancestrais na população referência foi de 924 animas, dos quais apenas 39 explicaram 50% da variabilidade genética da população.O coeficiente médio de relação foi estimado em 0,75%, sendo o maior coeficiente individual de 25%. O coeficiente de endogamia foi igual a zero de 1954 a 1984. Vale salientar que, neste período, estão incluídos os animais sem ascendência conhecida. A endogamia e o coeficiente médio de relação da população foram baixos, contudo podem estar subestimados em razão da pequena integralidade do pedigree.

In this study we used data from the 2558 pedigree cattle polled Gir born from 1954 to 2005. Analyses were performed using the Endog program. Of all animals studied, 61.86%, 10.56% and 0.10% had a pedigree in the first, second and third generation, respectively. The effective number of herds that provide breeding males was 10.25 for parents and 3.87 for grandparents, corroborating the low completeness of the pedigree. The number of founder animals was 975.5 and the effective number of founders were 141.34. The number of ancestors in the reference population was 924 animals from which only 39 accounted for 50% of the genetic variability of the population. The average relationship coefficient was estimated at 0.75%, the largest individual coefficient was 25%. The inbreeding coefficient was zero from 1954 to 1894. It is noteworthy that during this period included the population was low, but may be underestimated because of the small pedigree integrity.

Cloning, mapping and molecular characterization of porcine progesterone receptor membrane component 2 (PGRMC2) gene

Progesterone plays an important role in sow reproduction by stimulating classic genomic pathways via nuclear receptors and non-genomic pathways via membrane receptors such a progesterone receptor membrane component 2 (PGRMC2). In this work, we used radiation hybrid mapping to assign PGRMC2 to pig chromosome 8 and observed that this receptor has two transcripts in pigs. The full-length cDNA of the large transcript is 1858 bp long and contains a 669-bp open reading frame (ORF) encoding a protein of 223 amino acids. The shorter transcript encodes a protein of 170 amino acids. The porcine PGRMC2 gene consists of three exons 446 bp, 156 bp and 1259 bp in length. The promoter sequence is GC-rich and lacks a typical TATA box. Several putative cis-regulatory DNA motifs were identified in the 208-bp upstream genomic region. Five single nucleotide polymorphisms (SNPs) were detected in introns* and the 3' UTR. RT-PCR indicated that the PGRMC2 gene is expressed ubiquitously in all pig tissues examined.

Chromosome number and microsporogenesis of two accessions of Brachiaria dura Stapf (Poaceae) / Número de cromossomos e microsporogênese de dois acessos de Brachiaria dura Stapf (Poaceae)

The two accessions of B. dura analyzed (DU01 and DU02) are hexaploid (2n = 6x = 54), derived from x = 9. Meiotic abnormalities, such as precocious chromosome migration to the poles, laggards and micronuclei, were recorded in low frequency in both accessions. The few multivalent chromosome association at diakinesis and meiotic stability suggested that hexaploidy probably resulted from chromosome doubling. In DU02, chromosome transfer (cytomixis) among meiocytes, involving part or the entire genome was observed. The implication of these findings for the Brachiaria breeding is discussed.

Os dois acessos de B. dura analisados (DU01 e DU02) são hexaplóides (2n = 6x = 54), derivados de x = 9. Anormalidades meióticas como migração precoce de cromossomos para os polos, cromossomos retardatários e micronúcleos foram observados em baixa frequência em ambos os acessos. A presença de poucas associações cromossômicas em diacinese e a estabilidade meiótica sugere que a hexaploidia provavelmente resultou de duplicação cromossômica. No acesso DU02 observou-se transferência de cromossomos (citomixia) entre meiócitos, envolvendo parte ou todo o genoma. As implicações destes resultados para o melhoramento de Brachiaria são discutidas.

Restriction fragment analysis of the ribosomal DNA of Paratelmatobius and Scythrophrys species (Anura, Leptodactylidae)

Physical maps of the ribosomal RNA gene 28S of species belonging to the genera Paratelmatobius and Scythrophrys were constructed, using five restriction endonucleases. The restriction sites for Bam HI, Bgl II, Bst EII, and Eco RI had similar positions in all species, although there were interspecific differences in the size of the restriction fragments obtained. An additional Pvu II site was found in Scythrophrys specimens from Piraquara (State of Paraná, Brazil) and from Säo Bento do Sul (State of Santa Catarina, Brazil), but not in the Scythrophrys specimens from Rancho Queimado (State of Santa Catarina, Brazil). This finding is in agreement with the hypothesis regarding the existence of two species in the genus Scythrophrys. On the other hand, the extra Bst EII site considered in the literature to be a synapomorphy for the subfamilies Leptodactylinae and Telmatobiinae was not observed in the genera Paratelmatobius and Scythrophrys, which brings new questions about some taxonomic classifications that include Paratelmatobius in Leptodactylinae and Scythrophrys in Telmatobiinae. Interspecific variation was observed in the size of the restriction fragments analyzed and, in the case of group I Scythrophrys, there was also a variation between the individuals of the two populations. These data suggest that sequencing of the rDNA segments studied here may be useful in phylogenetic studies of the genera Paratelmatobius and Scythrophrys

Physical map and one-megabase sequencing of the human immunoglobulin lambda locus

O locus IGL humano está localizado no cromossomo 22q11.1-q11.2 e contém os genes responsáveis pelas cadeias leves de imunoglobulinas tipo lambda. Este locus foi recentemente mapeado (mapa físico) e seu 1 Mb DNA totalmente sequenciado. Neste revisäo focamos os principais resultados de caracterizaçäo dos genes v-lambda, sua localizaçäo cromossômica, a genômica e seqüenciamento do locus IGL.