Quantitative Trait Loci and Somatostatin
a quantitative trait and locus technology, applied in the field of quantitative trait loci and somatostatin, can solve the problems of reducing the ability of packers, inefficiency in management, processing and marketing of livestock, and not allowing optimal control of specific phenotypic characteristics related to meat eating quality, so as to improve feedlot performance and meat quality, increase or decrease the effect of marbling in the tissu
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example 1
[0201]A more precise chromosomal location for the SST locus was mapped using a genomic SST clone that was isolated by screening a bovine Bacterial Artificial Chromosome (BAC) library. The BAC library was screened and a genomic SST clone was isolated by using a 297 bp fragment that included exon 2 of the SST gene. Two primers, 5′-ACTTCTTGGCAGAGCTGCTGTC-3′ (SEQ ID NO:4) and 5′-ACGAGGGTCTTATTGAGGATTGG-3′ (SEQ ID NO:5), were used to amplify the SST fragment by PCR, using an annealing temperature 57° C. for 1 min (see Cai et al., Genomics 29:413-425 1995). The primers were designed based on the published nuclear DNA sequence of the SST gene (Accession No. U97077). Clone 36H7 was isolated from the BAC library, and DNA sequencing with an ABI 377 automated sequencer confirmed that the clone contained the 297 bp SST DNA fragment.
[0202]FISH analysis with the 36H7 clone demonstrated a strong, consistent signal on bovine chromosome 1 at region 1q32, thus localizing the SST gene to this region. ...
example 2
[0204]After the chromosomal location of the SST locus was mapped, a set of primers were designed to amplify and clone the genomic locus of the SST gene, including the bovine sequence for preprosomatostatin. The primers were designed to amplify different regions of the 2927 bp segment encompassing the 5′ untranslated region (5′UTR), two exons, and the intron sequence of the SST locus (SEQ ID NO:1). The primer sets used to amplify different portions of the 2927 bp segment were:[0205]Primer set 1: 5′-GCCTGGCTGGAGACAGGGTTAGTCATG-3′ (SEQ ID NO:8), nucleotides −1457 to −1431 of SEQ ID NO:1; and[0206]5′-CAGAAACCATCTACTAAACCCCA-3′ (SEQ ID NO:9), the reverse complement of nucleotides −910 to −888 of SEQ ID NO:1.[0207]Primer set 2: 5′-TAGGAGAGGCAAGGTTC-3′ (SEQ ID NO:10), nucleotides −96 to −80 of SEQ ID NO:1; and[0208]5′-CCAATAGATTAGCTCAATGTCCA-3′ (SEQ ID NO:11), the reverse complement of nucleotides 647 to 669 of SEQ ID NO:1.[0209]Primer set 3: 5′-GATCCCCGGCTCCGTCAGTTTCT-3′ (SEQ ID NO:12), n...
example 3
[0227]A series of statistical analyses were performed on the polymorphisms identified in the progeny of the Angleton Family Pedigree to determine the SST locations that are associated with desired traits in bovine. The data structure for each of the single loci in the complete data set are shown below:
GenotypeSSTmsC126TC157TT244CC575TG981A111362715509923161233329558325313522214548619070556Total614614614614614614
[0228]The Genotype designation of 11, 12, and 22 reflects the particular alleles of the SST locus present at the microsatellite or SNP location in an animal. For each of the above Genotype designations, the SNPs were designated as follows: genotype 11 is CC and genotype 22 is TT for C126T; genotype 11 is CC and genotype 22 is TT for C157T; genotype 11 is CC and genotype 22 is TT for T244C; genotype 11 is CC and genotype 22 is TT for C575T; and genotype 11 is AA and genotype 22 is GG for G981A. Animals with genotypes 11 and 22 are homozygous, and animals with genotype 12 are h...
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