Publications by authors named "Endang Tri Margawati"

Article Synopsis
  • This study analyzed runs of homozygosity (ROH) in Sumba Ongole bulls using genomic data to identify homozygous regions and inbreeding coefficients.
  • High-quality genomic data was processed using GenomeStudio and PLINK software, ensuring accurate filters, and resulted in the inclusion of over 25,000 SNP markers.
  • Results showed a presence of significant homozygous segments in specific autosomes, with an average inbreeding coefficient of 0.20, suggesting a history of inbreeding, potentially influencing traits relevant for adaptation and economics.
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Background: Sheep is one of the commodities of livestock which has been known widely in Indonesia for supporting the national food security. Improvement in genetic quality by selection based on genetic markers for growth is necessary to increase meat production. Quantitative trait loci (QTL) analysis in sheep suggests that Calpain 3 gene (CAPN3) gene might be one of the candidate loci affecting growth traits.

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Background: The cytochrome b (Cyt b) gene is one of the most studied mitochondrial DNA (mtDNA) genes to determine sheep's genetic profile. This study aimed to determine the genetic diversity and relationships of several Indonesian local sheep populations on Java Island, Indonesia, based on the mtDNA Cyt b gene sequences. Blood samples were collected from forty-one individual sheep in seven populations of Indonesia local sheep breeds on Java Island (Priangan = 6, Garut = 6, Batur = 7, Wonosobo = 5, Javanese Thin-Tailed/JTT = 7, Javanese Fat-Tailed/JFT = 5, and Sapudi = 5).

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Background: Bone morphogenetic protein receptor 1B (BMPR1B) gene is one of candidate genes for reproductive and growth traits in sheep. The present study was aimed to detect the Booroola (Fec) allele in BMPR1B gene and its association with growth traits in MEGA (Merino × Garut) sheep. A total of 82DNA samples collected from individual lamb (mixed-sex) blood were genotyped for allelic polymorphism using a PCR-RFLP method.

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One of small accessory genes between and is gene encoding TAT protein. This research was aimed to optimize the expression of Jembrana TAT (JTAT) protein with preparing () in advance using adopted methods of M1 (MgCl + CaCl) and M2 (CaCl + Glycerol). The best transformation efficiency resulting from a better transformation method was used to subsequent expression of JTAT protein.

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The objective of this research was to find the basic data on genetic diversity of mtDNA D-Loop in Aceh cattle and its association with Bhutanese, Chinese, and Indian cattle. There were sixty samples of DNA which had been sequenced; i.e.

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