Biology Unit 2 - Exam Revision Flashcards
Distinction between genes, alleles, and a genome
Genes: Basic units of heredity, consisting of DNA sequences that code for proteins, affecting physical and biochemical traits.
Alleles: Different variants of a gene; for example, a gene for flower colour may have a purple allele and a white allele.
Genome: The complete set of genetic instructions for an organism, encompassing all of its genes along with non-coding DNA.
Homologous chromosomes and their gene loci
Homologous chromosomes are pairs that contain the same genes at corresponding loci, but may have different alleles (e.g., one is inherited from the mother and the other from the father).
Difference between autosomes and sex chromosomes
Autosomes: Non-sex chromosomes that determine traits unrelated to sex (e.g., chromosome pairs 1-22 in humans).
Sex chromosomes: Chromosomes that determine sexual characteristics (e.g., X and Y chromosomes).
Variability in size and number of chromosomes in different organisms
E.g, Humans have 46 chromosomes, while fruit flies have 8. The number and structure of chromosomes can vary widely between species, affecting genetic information.
Karyotypes and identification of chromosome abnormalities
A karyotype is a comprehensive display of an organism’s chromosomes arranged by size and shape. Karyotypes can be used to identify genetic disorders such as Down syndrome (47, XX or XY +21), characterised by the presence of an extra copy of chromosome 21.
Meiosis and its role in producing haploid gametes from diploid cells
Meiosis is a two-staged cell division process (Meiosis I and II) that reduces the chromosome number by half, producing four haploid gametes (sperm or eggs) from one diploid cell.
Significance of crossing over and independent assortment in genetic diversity
- Crossing over allows for the exchange of genetic material between homologous chromosomes during prophase I of meiosis, increasing genetic variation.
- Independent assortment occurs in metaphase I, where chromosomes are distributed to daughter cells independently of one another, resulting in a mix of maternal and paternal chromosomes in gametes.
Use of symbols to write genotypes
Genotypes are represented using symbols, where uppercase letters signify dominant alleles (e.g., A) and lowercase letters signify recessive alleles (e.g., a).
Expression of dominant and recessive phenotypes (including codominance and incomplete dominance)
An organism with at least one dominant allele (e.g., AA or Aa) expresses the dominant phenotype, while organisms with two recessive alleles (aa) express the recessive phenotype.
Codominance occurs when both alleles in a heterozygous individual contribute equally to the phenotype (e.g., AB blood type).
Incomplete dominance results in a blended phenotype (e.g., pink flowers from red (RR) and white (WW) parents).
Influence of genetic material, environment, and epigenetic factors on phenotypes
Genetic makeup provides the blueprint for traits, but environmental influences (e.g., sunlight, nutrition) and epigenetic modifications (e.g., DNA methylation) can alter gene expression, leading to variations in phenotypes.
Pedigree charts and patterns of inheritance (autosomal and sex-linked)
Pedigree charts illustrate the inheritance of traits across multiple generations, allowing examination of autosomal traits (inherited via non-sex chromosomes) and sex-linked traits (associated with genes on sex chromosomes like colour blindness, which is X-linked).
Predicted genetic outcomes for monohybrid crosses
Monohybrid crosses consider one trait (e.g., flower colour) and utilise a Punnett square to predict ratios of expected genotypes (1 homozygous dominant: 2 heterozygous: 1 homozygous recessive) and phenotypes in the offspring.
Linked genes vs. independent assortment in inheritance predictions
Genes located close together on the same chromosome are said to be linked, leading to fewer recombinant offspring. In contrast, independently assorting genes generate a variety of combinations.
Biological advantages and disadvantages of asexual reproduction
Asexual reproduction (e.g., binary fission in bacteria) enables rapid reproduction and colonisation, resulting in large populations. However, it yields little genetic diversity, making populations vulnerable to diseases and environmental changes.
Biological advantages of sexual reproduction, especially in promoting genetic diversity
Sexual reproduction leads to increased genetic variability through the mixing of parental genes, which enhances the adaptability of populations in a changing environment and allows for natural selection to act on more diverse traits.