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Transcript
“Cowboy Glossary” of Genetic Terms
The terms and jargon used in genetic research
can be confusing and overwhelming. Below is a
simple “cowboy glossary” of commonly used terms
in the discussion of genomic-enhanced EPDs.
This is not a comprehensive glossary and was
purposely put in an order other than alphabetical
to help aid in the understanding the genetic terms
as they relate to one another.
Genetics – the division of science that studies
genes, heredity and the relationships among living
organisms
Genomics – a specific discipline in genetics that
studies genomes
Genome – the total genetic material in an
organism, encoded in DNA or RNA
DNA – deoxyribose nucleic acid, present in
the nucleus of the cells in all living organisms
and contains all the genetic information of the
organism; a molecule of DNA is formed by a
double strand of millions of nucleotides joined
together
Base pairs – the backbone of DNA strands, the
order of which along a DNA strand accounts for
the genetic variation between animals, in both
the function and differences of genes; the most
common bases are always paired up in the same
way: Adenine (A) bonds with Thymine (T); Cytosine
(C) bonds with Guanine (G)
Genetic code – the sequence of bases within DNA,
made up of triplets (a group of three bases)
Gene – the sequence of triplets (three bases) in the
DNA molecule; one gene may contain a thousand
or more bases
Genetic markers – pieces of DNA (information),
either a single gene or a sequence of genes,
identified on a specific location on a chromosome;
the identified markers influence a specific trait or
several traits
Chromosome – the organized structure of DNA
and protein found in cells, containing many genes
in a single piece of coiled DNA; cattle have 30
chromosomes
38 | MARCH 2016
Allele – a pair or more of genes located on a
specific position on a chromosome
Loci – the specific place on a chromosome where a
gene is located
SNP – Single-nucleotide polymorphism
(pronounced ‘snip’), a specific DNA marker; a
panel of critically selected SNPs for multiple
traits identifies the approximate location of DNA
sequences having a direct effect on a trait or series
of traits
50K SNP – the bovine 50K chip which provides
information on 50,000 locations (SNPs) throughout
the genome; these 50,000 markers are used to
create MBVs for genomic-enhanced EPDs.
Low Density Genomic Profile – a DNA test that
uses 30,000 SNP markers; these 30K markers are
then imputed up to 50K for GE-EPDs
High Density Genomic Profile – a DNA test
that uses 150,000 SNP markers, providing more
genomic information; GE-EPDs are created by
extracting 50K of these markers
Genetic variance (GV) – variation in phenotypes
due to the presence of different genotypes in a
population
Genetic tests – tools that can be used to identify
genetic markers, which lead to predicting an
animal’s performance potential
Molecular Breeding Value (MBV) – a prediction
of value for a certain trait derived from genomes
(information from SNPs)
Genomic-enhanced EPDs – combining DNA
markers with individual animal, pedigree and
progeny data into one EPD calculations; also
referred to as marker-assisted EPDs (MA EPDs) or
molecular breeding value EPDs (MBV EPDs)
Marker Assisted Selection (MAS) – the use of one
or a few genetic markers to assist in the selection
of desirable traits
National Cattle Evaluation – incorporating
performance measures from individual animals,
progeny, and pedigree relationships to generate a
metric (expected progeny differences, EPDs) that
can be to make selection decisions LW