How is DNA organized?
§ DNA is stored in the nucleus of cells,
and it’s the cells genetic information.
§ A gene is a section of DNA that codes
for one protein.
§ A chromosome is a long length of
DNA which carries genetic information
in the form of genes.
Diploid vs Haploid
§ A diploid nucleus is a nucleus that
contains two sets of chromosomes.
This means 23 pairs (so 46 in total)
§ All of your normal somatic cells are
diploid
§ A haploid nucleus is a nucleus that
contains one set of chromosomes.
This means 23 chromosomes only.
§ Gametes (sperm/egg cells) are haploid
Mitosis
§ Mitosis is a nuclear division giving rise
to genetically identical cells
§ Mitosis is needed for growth, repair of
damaged tissues and cell
replacement. It is also used for
asexual reproduction in some
organisms.
Mitosis: The steps
§ Step 1: Duplicate the chromosomes
§ Step 2: Line up the chromosomes
along the centre
§ Step 3: Separate the chromosomes
§ Step 4: Nucleus divides
§ Step 5: Cytoplasm divides
§ This creates diploid cells
Stem cells
§ Stem cells are undifferentiated cells
that divide asymmetrically by mitosis to
produce specialized cells
§ Almost all cells in the body have the
same DNA, but they become
specialized because some genes are
switched on and some are switched
off.
Meiosis
§ Step 1: Duplicate the chromosomes
§ Step 2: Line up the chromosomes
along the centre
§ Step 3: Separate the chromosomes
§ Step 4: Nucleus divides
§ Step 5: Cytoplasm divides
§ Step 6: Nuclei divide again
§ Step 7: Cytoplasm divides again
§ This creates haploid gametes
How does this build on what you already know?
How does link to the rest of biology?
§ A gene is a section of DNA that
codes for a protein
§ These proteins could be anything
including enzymes, hormones,
neurotransmitters and cell membrane
carrier proteins
Let’s look closer - Transcription
§ Each three bases of DNA is called a
triplet.
§ An enzyme will come along, unzip
the DNA strands so the bases are
exposed, and transcribe a
complimentary strand of mRNA.
§ mRNA is a lot like DNA, but it uses
the letter U instead of T.
§ This process is called transcription.
§ This is so DNA stays in the
nucleus.
Let’s look closer - Translation
§ Each three bases of mRNA is called a
codon.
§ The mRNA will move out of the nucleus
into the cytoplasm, and attach to a
ribosome.
§ The ribosome will read the code and
choose the correct amino acid for each
codon.
§ Each codon codes for a different amino
acid, and there are 20 amino acids in
total.
§ The ribosomes assembles the amino
acids into proteins.
Overview
What are alleles?
§ Every person has two versions of
every gene.
§ These versions of genes are called
alleles
§ Inheritance is the passing on of
genes to the next generation
There are two types of alleles
§ An allele is either dominant or
recessive.
§ If a person has a dominant allele, it will
always be expressed
§ If a person has a recessive allele, it will
only be expressed if there is no
dominant
What are the combinations?
§ This means for each gene, you can
either have 2 dominant alleles, 2
recessive alleles, or one of each.
§ Homozygous dominant means you
have 2 dominant alleles
§ Homozygous recessive means you
have 2 recessive alleles
§ Heterozygous means you have 1
dominant and 1 recessive allele
Genotype vs phenotype
§ The genotype of an individual is
whether they are homozygous
dominant, homozygous recessive or
heterozygous for a particular gene
§ The phenotype of an individual is the
characteristic you can see in the
organism
Punnett squares
§ We can use Punnett squares to
predict the genotypes and phenotypes
of the offspring when two individuals
mate
Sex inheritance
§ The 23rd pair of chromosomes are the
sex chromosomes
§ If you are female you have 2 X
chromosomes
§ If you are male you have 1 X and 1 Y
chromosome
§ This means males determine the sex of
the offspring
Genetic diagrams
Pedigree diagrams
What is codominace?
§ Sometimes, the alleles for a gene
can be codominant which means in
a heterozygote, both alleles are
expressed.
What are blood groups?
§ Blood groups can show
codominance.
§ The alleles are IA (for group A), IB (for
group B) and I (for group O).
Sex linkage
§ Sex linkage is where a gene is
located on a sex chromosome.
§ This means a trait or disease may be
more likely to be passed on to a
specific sex
§ A disease can be X-linked or Y-linked
Sex linkage
§ Red-green
colourblindness is an X-
linked recessive disorder
§ This means males are
more likely to have it has
they only have one X
chromosome.

Inheritance for IGCSE students 0610 .pdf

  • 1.
    How is DNAorganized? § DNA is stored in the nucleus of cells, and it’s the cells genetic information. § A gene is a section of DNA that codes for one protein. § A chromosome is a long length of DNA which carries genetic information in the form of genes.
  • 2.
    Diploid vs Haploid §A diploid nucleus is a nucleus that contains two sets of chromosomes. This means 23 pairs (so 46 in total) § All of your normal somatic cells are diploid § A haploid nucleus is a nucleus that contains one set of chromosomes. This means 23 chromosomes only. § Gametes (sperm/egg cells) are haploid
  • 3.
    Mitosis § Mitosis isa nuclear division giving rise to genetically identical cells § Mitosis is needed for growth, repair of damaged tissues and cell replacement. It is also used for asexual reproduction in some organisms.
  • 4.
    Mitosis: The steps §Step 1: Duplicate the chromosomes § Step 2: Line up the chromosomes along the centre § Step 3: Separate the chromosomes § Step 4: Nucleus divides § Step 5: Cytoplasm divides § This creates diploid cells
  • 5.
    Stem cells § Stemcells are undifferentiated cells that divide asymmetrically by mitosis to produce specialized cells § Almost all cells in the body have the same DNA, but they become specialized because some genes are switched on and some are switched off.
  • 6.
    Meiosis § Step 1:Duplicate the chromosomes § Step 2: Line up the chromosomes along the centre § Step 3: Separate the chromosomes § Step 4: Nucleus divides § Step 5: Cytoplasm divides § Step 6: Nuclei divide again § Step 7: Cytoplasm divides again § This creates haploid gametes
  • 7.
    How does thisbuild on what you already know? How does link to the rest of biology? § A gene is a section of DNA that codes for a protein § These proteins could be anything including enzymes, hormones, neurotransmitters and cell membrane carrier proteins
  • 8.
    Let’s look closer- Transcription § Each three bases of DNA is called a triplet. § An enzyme will come along, unzip the DNA strands so the bases are exposed, and transcribe a complimentary strand of mRNA. § mRNA is a lot like DNA, but it uses the letter U instead of T. § This process is called transcription. § This is so DNA stays in the nucleus.
  • 9.
    Let’s look closer- Translation § Each three bases of mRNA is called a codon. § The mRNA will move out of the nucleus into the cytoplasm, and attach to a ribosome. § The ribosome will read the code and choose the correct amino acid for each codon. § Each codon codes for a different amino acid, and there are 20 amino acids in total. § The ribosomes assembles the amino acids into proteins.
  • 10.
  • 11.
    What are alleles? §Every person has two versions of every gene. § These versions of genes are called alleles § Inheritance is the passing on of genes to the next generation
  • 12.
    There are twotypes of alleles § An allele is either dominant or recessive. § If a person has a dominant allele, it will always be expressed § If a person has a recessive allele, it will only be expressed if there is no dominant
  • 13.
    What are thecombinations? § This means for each gene, you can either have 2 dominant alleles, 2 recessive alleles, or one of each. § Homozygous dominant means you have 2 dominant alleles § Homozygous recessive means you have 2 recessive alleles § Heterozygous means you have 1 dominant and 1 recessive allele
  • 14.
    Genotype vs phenotype §The genotype of an individual is whether they are homozygous dominant, homozygous recessive or heterozygous for a particular gene § The phenotype of an individual is the characteristic you can see in the organism
  • 15.
    Punnett squares § Wecan use Punnett squares to predict the genotypes and phenotypes of the offspring when two individuals mate
  • 16.
    Sex inheritance § The23rd pair of chromosomes are the sex chromosomes § If you are female you have 2 X chromosomes § If you are male you have 1 X and 1 Y chromosome § This means males determine the sex of the offspring
  • 17.
  • 18.
  • 19.
    What is codominace? §Sometimes, the alleles for a gene can be codominant which means in a heterozygote, both alleles are expressed.
  • 20.
    What are bloodgroups? § Blood groups can show codominance. § The alleles are IA (for group A), IB (for group B) and I (for group O).
  • 21.
    Sex linkage § Sexlinkage is where a gene is located on a sex chromosome. § This means a trait or disease may be more likely to be passed on to a specific sex § A disease can be X-linked or Y-linked
  • 22.
    Sex linkage § Red-green colourblindnessis an X- linked recessive disorder § This means males are more likely to have it has they only have one X chromosome.