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1.
Front Genet ; 14: 1318679, 2023.
Article in English | MEDLINE | ID: mdl-38075675

ABSTRACT

Introduction: Body measurement traits are integral in cattle production, serving as pivotal criteria for breeding selection. Wenshan cattle, a local breed in China's Yunnan province, exhibit remarkable genetic diversity. However, the molecular mechanisms regulating body measurement traits in Wenshan cattle remain unexplored. Methods: In this study, we performed a genome-wide association method to identify genetic architecture for body height body length hip height back height (BAH), waist height and ischial tuberosity height using the Bovine 50 K single nucleotide polymorphism Array in 1060 Wenshan cattles. Results: This analysis reveals 8 significant SNPs identified through the mixed linear model (MLM), with 6 SNPs are associated with multiple traits and 4 SNPs are associated with all 6 traits. Furthermore, we pinpoint 21 candidate genes located in proximity to or within these significant SNPs. Among them, Scarb1, acetoacetyl-CoA synthetase and HIVEP3 were implicated in bone formation and rarely encountered in livestock body measurement traits, emerge as potential candidate genes regulating body measurement traits in Wenshan cattle. Discussion: This investigation provides valuable insights into the genetic mechanisms underpinning body measurement traits in this unique cattle breed, paving the way for further research in this domain.

2.
Protein Expr Purif ; 109: 35-9, 2015 May.
Article in English | MEDLINE | ID: mdl-25644541

ABSTRACT

This paper reports the successful expression of a lactoferrin gene-obtained from the mammary gland tissue of Tibetan sheep-in the yeast Pichia pastoris GS115 using pPICZαA as the recombinant plasmid and α-factor signal sequence for secretion. The recombinant lactoferrin was purified by ammonium sulfate precipitation, ion-exchange column chromatography and gel-filtration chromatography, and it had a molecular mass of 76kDa. We obtained an expression yield of >60mgL(-1) and specific activity of 2533.33Umg(-1). The antimicrobial activities and iron-binding behaviors of recombinant lactoferrin indicated that it was correctly folded and functional. Additionally, recombinant lactoferrin inhibited the growth of Escherichia coli JM109 and Staphylococcus aureus. These findings indicate that recombinant lactoferrin is a potential antibiotic for use on humans. This study also demonstrates the successful expression of recombinant lactoferrin using the eukaryotic host organism P. pastoris, paving the way for protein engineering using this gene.


Subject(s)
Cloning, Molecular/methods , Gene Expression , Lactoferrin/isolation & purification , Lactoferrin/metabolism , Mammary Glands, Animal/metabolism , Saccharomyces cerevisiae/metabolism , Animals , Anti-Bacterial Agents/pharmacology , DNA, Complementary/genetics , Electrophoresis, Agar Gel , Electrophoresis, Polyacrylamide Gel , Female , Hydrogen-Ion Concentration , Iron/metabolism , Lactoferrin/pharmacology , Microbial Sensitivity Tests , Protein Binding/drug effects , Recombinant Proteins/isolation & purification , Recombinant Proteins/pharmacology , Sequence Analysis, DNA , Sheep , Staphylococcus aureus/drug effects , Staphylococcus aureus/growth & development
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