Chapter 18: Inheritance Flashcards
1
Q
Inheritance
A
- the transmission of traits from one generation to another
2
Q
Gene
A
- a sequence of DNA nucleotides that controls the formation of a single polypeptide. it is also a unit of inheritance
3
Q
Alleles
A
- different forms of the same genes
- alleles occupy the same relative position on a pair of homologous chromosomes
4
Q
Genotypes
A
- the combination of alleles for a particular gene
5
Q
Phenotype
A
- expressed trait or outwards appearance is called phenotype
6
Q
Homozygous
A
- refers to having 2 identical alleles of a particular gene
7
Q
Heterozygous
A
- refers to having 2 different alleles of a particular gene
8
Q
Codominant alleles
A
- in codominance, both alleles express themselves in the heterozygote, which has a phenotype intermediate between that of its pure-bred parents. Alleles are said to be codominant
9
Q
Chromosomes in human body
A
- there is 1 pair of sex chromosomes and 22 pairs of non-sex chromosomes called autosomes
- human body cells are diploid with 23 pairs of chromosomes (46 chromosomes in total)
- in males, there is one X and one shorter Y chromosome in each body cell
- in females, there is a pair of X chromosomes in each normal body cell
10
Q
Variation
A
- refers to the differences in traits between individuals of the same species
11
Q
Discontinuous variation
A
- traits show clear-cut phenotypes with no intermediate form between the traits
- traits are easily distinguishable and are not affected by environmental conditions
- controlled by one or a few genes
- genes do not shows addictive effect
- relatively unaffected by environmental conditions
- ex: blood group
12
Q
Continuous variation
A
- brought about the combined or addictive effects of many genes
- involves a range of phenotypes
- controlled by many genes
- genes show addictive effects
- greatly affected by environmental conditions
- ex: skin colour
13
Q
Sources of genetic variation
A
- meiosis, since they produce genetically dissimilar gametes with different combinations of parental chromosomes
- random fertilisation
- mutation
14
Q
Mutation
A
- a change in the sequence of a gene or in the chromosome number
15
Q
Albinism
A
- example of gene mutation
- when they are homozygous for the albinism allele are albinos
- they have reddish-white skin and white hair
- the iris does not contain any pigment, so it will appear red because of the colour of the blood vessels in it