Chapter 18: Inheritance Flashcards
(40 cards)
Define inheritance.
Inheritance refers to the transmission of traits from one generation to another.
What is a hereditary trait?
A hereditary trait is a characteristic that can be passed on from one generation to another.
What are some examples of hereditary traits?
(8 pts.)
- Hair type
- Shape of earlobe
- Eye color
- Face shape
- Chin shape
- Ability to roll tongue
- Skin colour
- Blood type
What is monohybrid inheritance?
Monohybrid inheritance refers to the inheritance of one characteristic with two contrasting forms.
Each characteristic is controlled by a single gene, consisting of a pair of alleles.
Define the term ‘allele’.
Alleles are:
- different forms of a gene that
- occupy the same relative positions on a pair of homologous chromosomes
Define the term ‘gene’.
A gene is a:
- unit of inheritance, born on a particular locus of a chromosome
- segment of DNA containing a sequence of nucleotides which code for a single polypeptide
How do alleles affect genetic variation?
Different alleles can lead to variations in traits among individuals.They contribute to the genetic diversity within a population.
Describe a chromosome.
- rod-like structures visible in the nucleus during cell division
- made up of DNA molecule
What is phenotype in genetics?
- observable traits
- influenced by the organism’s genotype and environmental factors.
What is genotype in genetics?
- genetic makeup of an organism inherited from its parents
- determines the specific traits that can be expressed in the phenotype.
What is homozygous in genetics?
Homozygous refers to having two identical alleles for a particular gene.
What is heterozygous in genetics?
Heterozygous refers to having two different alleles for a particular gene.
Explain the term ‘dominant allele’.
A dominant allele is an allele that expresses itself in both homozygous dominant and heterozygous conditions.
Explain the term ‘recessive allele’
A recessive allele is an allele that will only express itself in a homozygous recessive genotype.
Define co-dominance.
Co-dominance refers to when two different alleles of the same genotype are equally expressed in its phenotype.
With reference to ABO blood group phenotypes, explain what is meant by co-dominance.
- co-dominance is when two different alleles of the genotype are both expressed evenly in its phenotype
- in the ABO blood group, the alleles IA and IB are codominant
- in an individual with both of these alleles, with a heterozygous IA IB genotype
- both alleles are expressed in its phenotype
- both the antigens A and B are found on the red blood cells
- both of these alleles IA and IB are dominant over the IO allele and will be expressed over the IO allele in the heterozygous individual;
What is the Law of Segregation?
Each gamete will only contain one factor for a characteristic
How do dominant and recessive alleles affect phenotype?
Dominant alleles can mask the expression of recessive alleles in the phenotype.The presence of at least one dominant allele typically results in the dominant trait being expressed.
What are the key differences between discontinuous and continuous variation?
Discontinuous variation: involves a few clear-cut phenotypes
Continuous variation: involves a range of phenotypes
Discontinuous variation: controlled by one or a few genes
Continuous variation: controlled by many genes
Discontinuous variation: not affected by environmental conditions
Continuous variation: affected by environmental conditions
What are the sources of genetic variation?
- Meiosis
- produces genetically dissimilar gametes with different combinations of parental chromosomes. - Random fertilization
- allows any sperm to fuse with an egg, creating genetic diversity - Mutation
- a change in the sequence of a gene or in chromosome number or structure.
Define mutation.
A mutation is a sudden, random change in the DNA structure or chromosomal structure.
What are the main causes of mutations in biology?
- Errors during the replication of genes or chromosomes
- Dominant mutations are easily detected, while recessive mutations may remain undetected for generations.
What are the two main types of mutations?
- Chromosome mutation
- Gene mutation
What is a chromosome mutation and what condition can it cause?
- Change in the structure or number of chromosomes
- Condition:
-Down syndrome, where individuals have a third copy of chromosome 21.