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Complementary Base Pairs
A (Adenine) pairs with T (Thymine)
G(Guanine) pairs with C (Cytosine)
Chromatin
Loosly wound DNA and Proteins for Organization
Chromosome
Chromatin when packed up super tightly and super coiled for protection during cell division
Genome
An instruction manual for making biological structures. It contains all the information necessary for the growth, development, and functioning of that organism.
Coding Region
The part of a gene that contains the coding sequences for proteins, which are translated into functional products.
Non Coding Region
The segment of a gene that does not code for proteins. Non-coding regions can regulate gene expression and may have other functional roles.
Gene
A nucleic acid sequence that encodes one functional protein
What is the sequence of DNA, transcription and translation?
The process by which the genetic information in DNA is transcribed into RNA, and then translated into a specific sequence of amino acids to form a protein.
Transcription from DNA to mRNA
is the first step in gene expression, where the DNA sequence is copied into a complementary RNA sequence.
RNA complementary base strand
that pairs with the DNA template strand during transcription, following base pairing rules. A pairs with U and G pairs with C
Exons
Coding Regions
Intron
Non Coding regions that get removed during splicing
Ribosomes
Cellular structures that synthesize proteins by translating messenger RNA.
Translation into protein
is the process where ribosomes decode mRNA sequences to produce polypeptides, which then fold into functional proteins.
Codon
each set of three nucleotides code for a particular amino acid
Genetic Mutation
A change in the nucleotide sequence of a genome
Spontaneous Mutation
A mutation that occurs inside of the cell with no external disruptions
Damage from environment
causes changes in DNA that can lead to mutations. Changes externally (Radiation, chemicals, and viruses)
Replication Errors
Mistakes made during DNA replication that can result in mutations if not corrected such as deletion, insertion, and substitution.
Allele
Different variants of a gene
Gene Locus
The position of a certain gene on a chromosome
Synonymous Substitution
Nucleotide Substitution that does not change the amino acid sequence.
Non-Synonymous Substitution
Nucleotide substitution that alters the amino acid sequence.
Diploid organisms
Two pairs of homologous Chromosomes
-Same characteristics and same name
-One from the mother and one from the father
-Same genes
Homozygous Dominant
AA
Homozygous Recessive
aa
Heterozygous
Aa
Dominant Allele
An allele that expresses its phenotype in the presence of another allele, often represented by a capital letter.
Recessive Allele
An allele that expresses its phenotype only when two copies are present, often represented by a lowercase letter.
Genotype
an individuals combination of alleles at one or more gene locus’s
Phenotype
observable traits of an organism
Traits or charactersitics
Any observable characteristics of an organism
Phenotype
A variant of a trait expressed by the genotype
Blended Inheritance
offspring that are a mix of their parents traits
Discrete Inheritance
Traits that are inherited independently and show distinct categories without blending.
Concept of Dominance
If an individual has at least one copy of the dominant allele for a trait, that trait will be expressed in the phenotype.
Individuals with two copies of the recessive allele with show the recessive phenotype.
Principles of Segregation
The Principle of Segregation states that during the formation of gametes, the two alleles responsible for a trait separate from each other. This means each gamete carries only one allele for each trait.
Incomplete Dominance
Not one allele is more dominant over the other. Instead, the resulting phenotype is a blend of both alleles, resulting in an intermediate expression.
No linkage between loci
The Probability of producing BT=bT
Linkage between loci
Probability of producing BT>bT