HEREDITY Flashcards

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1
Q

What are the key differences between sexual and asexual reproduction in terms of genetic variation and reproductive processes?

A

Sexual reproduction:
- Involves two parents and the production/fusion of male and female gametes.
- Requires meiotic division followed by mitotic division.
- Results in offspring with genetic variation, containing characteristics from both parents.
- Greater ability to adapt to changing environmental conditions.
Asexual reproduction:
- Involves only one parent and no production or fusion of gametes.
- Requires only mitotic division.
- Offspring are genetically identical to the parent (clones).
- less gene variation, reduced adaptability to environmental changes.

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2
Q

What are the advantages and disadvantages of internal and external fertilisation?

A

Internal fertilisation:
- Occurs inside the female reproductive tract.
- Negatives:
- Fewer female gametes and many male gametes produced.
- Parental care is often provided for eggs or offspring.
- Positives:
- Higher chances of fertilisation
- Reduced risks from predators and environmental threats.
- Examples: mammals.
External fertilisation:
- Occurs outside the female reproductive tract, typically in water to prevent desiccation.
- Positives:
- Large numbers of both male and female gametes are produced.
- No parental care provided.
- Negatives:
- Lower chances of fertilisation.
- Offspring are often left vulnerable
- Examples: amphibians, fish.

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3
Q

What are the advantages and disadvantages of asexual reproduction in plants?

A

Advantages:
- Rapid multiplication, allowing for quick growth and seed production to aid dispersal.
- Increased survival chances after extreme events (e.g., bushfires, cold) as no mating is required.
- Lower energy requirement for reproduction since only one parent is needed.
Disadvantages:
- Lack of genetic variation, making the population more vulnerable to diseases or environmental changes.
- Overcrowding and competition due to limited or no seed dispersal mechanisms.

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4
Q

What are the key stages and processes involved in sexual reproduction in plants?

A

Pollination:
- The male part, stamen (anther and filament), produces pollen.
The female part, pistil (stigma, style, ovary), receives pollen on the stigma.
Pollen is transferred to the stigma by external agents like wind, water, animals.
- Cross-pollination increases genetic variation, while self-pollination ensures reproduction without external agents.
Fertilisation:
- Pollen travels down the style to fertilise the ovule inside the ovary, forming a zygote.
- The fertilised ovule becomes a seed containing the embryo.
Seed Dispersal:
- Seeds are dispersed by abiotic agents (e.g., wind, water) or biotic agents (e.g., animals).
-Dry fruits are usually dispersed by abiotic agents; fleshy fruits by biotic agents.
Germination:
- Seed germinates when conditions (water, oxygen, warmth) are suitable.
- The embryo grows into a young plant, eventually maturing to restart the reproductive cycle

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5
Q

What are the different methods of reproduction in fungi, and how do they ensure the continuity of the species?

A

Budding:
- A small bud forms and detaches from the parent, creating a new individual.
Fast reproduction, no mate needed, but no genetic variation.
Asexual Spore Reproduction:
- Spores are produced and dispersed, growing into new fungi.
Rapid reproduction and wide colonisation, but offspring are genetically identical.
Sexual Spore Reproduction:
- Haploid hyphae fuse, creating genetically diverse spores.
Increases genetic variation, allowing adaptation to environmental pressures.

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6
Q

What are the different methods of reproduction in bacteria and how do they ensure the continuity of the species?

A

Binary fission
- DNA is replicated.
- The cell elongates and divides via cytokinesis.
- Two genetically identical daughter cells are produced.
Ensures Continuity:
- Fast reproduction
- No mate required: time and energy, efficient.
Limitations:
- Lack of genetic diversity, but high mutation rates during DNA replication can introduce some variability.

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7
Q

How has understanding plant and animal reproduction been applied in artificial reproduction to improve agricultural yields?

A

Method: Hand pollination by dusting pollen onto the stigma –> increases yield, boosts genetic variability.
- Labour-intensive, decreased genetic diversity with overuse.

Method: Collection, freezing, insertion of semen –> higher quality offspring, increased food production, conservation
Costly, long time, overuse–>reduce diversity .

Method: cuttings, bulbs, tubers, grafting –> produces clones with desirable traits (disease resistance)
- less genetic diversity, vulnerability to disease+selection pressures.

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8
Q

What are all the steps for mitosis?

A

Interphase, prophase, metaphase, anaphase, telophase, cytokenesis

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9
Q

What are the main functions of mitosis?

A
  • increase body cells for growth
  • replace ‘worn out’ cells
  • repair damaged cells
  • asexual reproduction
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10
Q

What are all the steps for meiosis?

A

Early prophase, late prophase, metaphase I, anaphase I, telophase I, cytokenesis I, metaphase II, anaphase II, telophase II, cytokenesis II

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11
Q

What are the main functions of meiosis?

A
  • produces haploid sex cells with half the chromosome number of somatic cells.
  • Increases genetic diversity through crossing over and independent assortment –> unique combinations of alleles.
  • Maintains a stable chromosome number across generations when gametes fuse during fertilisation.
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12
Q

What are the components of a DNA nucleotide?

A

deoxyribose sugar, phosphate, nitrogenous base

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13
Q

What are nitrogenous bases held together by?

A

Weak hydrogen bonds which are easy to pull a part when replicating DNA.

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14
Q

What are the components of a RNA nucleotide?

A

ribose sugar, phosphate, nucleotide

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15
Q

how does mitosis effect continuity of species?

A
  • growth+repair –> survival
  • asexual reproduction
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16
Q

how does meiosis effect continuity of species

A
  • produces haploid sex cells with half the chromosome number of somatic cells.
  • crossing over and independent assortment, resulting in unique combinations of alleles –> genetic diversity
  • maintains a stable chromosome number across generations when gametes fuse during fertilisation
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17
Q

how does DNA replication effect continuity of species

A

correct DNA replication –> correct proteins are made that are essential for survival

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18
Q

characteristics of DNA in prokaryotes

A
  • DNA in cytoplasm as lack a nucleus.
  • single circular chromosome containing all genomic DNA.
  • contain plasmids: small, circular extrachromosomal DNA segments carry additional genes.
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19
Q

How is DNA organised in eukaryotic cells?

A
  • Genomic DNA is stored within chromosomes inside the nucleus.
  • Consists of multiple pairs of linear chromosomes, allowing greater genetic variation through sexual reproduction.
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20
Q

What are the key steps for transcription?

A
  1. RNA polymerase attaches itself to the promoter.
  2. DNA unwinds –> separate only at the part of DNA that contains the gene to be used.
  3. Non-coding strand of DNA –> complementary mRNA.
  4. In eukaryotes, transcribed mRNA is called pre-mRNA. Pre-mRNA contains coding sequences of nucleotides called exons –> amino acids. Between these exons are sequences of nucleotides called introns –> mRNA is spliced
  5. After splicing –> mature mRNA is formed –> mRNA moves from the nucleus to the cytoplasm for translation to occur.
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21
Q

Where does transcription and translation occur?

A

Transcription occurs in the cytoplasm, translation occurs in ribosome

22
Q

What are the key steps for translation?

A

Ribosomes match tRNA anticodons with mRNA codons. tRNA carries specific amino acids, released upon pairing.
Amino acids join via peptide bonds to form a polypeptide chain.
Polypeptide chain folds or binds with others to form a functional protein.

23
Q

What is the role of mRNA in protein synthesis?

A
  • single stranded RNA transcribed from a DNA template.
  • carries codon triplets with instructions for amino acid assembly.
    mRNA is transcribed from DNA, carrying the gene’s instructions to the ribosome.
  • ensures mRNA codons pair with tRNA anticodons, assembling amino acids in the correct sequence.
  • forms a polypeptide chain that folds into a functional protein.
24
Q

What is the role of tRNA in protein synthesis?

A
  • anticodon on one end and specific amino acid on the other.
  • ensures each amino acid added to the polypeptide chain matches the mRNA codons during translation.
  • carries only one type of amino acid, determined by its anticodon sequence.
  • correct amino acid sequence allows proper protein folding
  • errored sequence –> misfolded, non-functional proteins.
25
Q

What is the role of polypeptide synthesis in an organism?

A
  • polypeptide chain –> functional protein
  • organism function + development - each protein performs specific roles
26
Q

How do genes and the environment influence phenotypic expression?

A
  • Genotype: genes determine trait
  • Phenotype: Physical observable trait
    Gene Expression: Genes switched on/off –> produce proteins that determine phenotype.
  • Incorrect gene sequences –> non-functional proteins.
  • Nature vs. Nurture
  • Environment modifies gene expression, affecting phenotype.
27
Q

function+eg of structural protein

A
  • provides support
  • collagen+elastin in skin
28
Q

function+eg of structural hormonal

A
  • signalling proteins –> cell to communication –> coordinate activities in the body
  • insulin regulates blood glucose level
29
Q

function+eg of structural enzymes

A
  • catalyse metabolic reactions in the body
  • amylase breaks down starch in the mouth and pancreas during
    digestion.
30
Q

function+eg of transport proteins

A
  • carry substances around the body
  • haemoglobin binds to oxygen and transports to cells through the
    blood
31
Q

function+eg of immunoproteins

A
  • protects against disease causing organisms
  • antibodies identify foreign materials in body for removal
32
Q

function+eg of immunoproteins

A
  • voluntary and involuntary movement
  • actin and myosin slide over one another –> muscle contraction.
33
Q

function+eg of storage proteins

A
  • store mineral irons in the body
  • ferritin –> regulates iron stored in body.
34
Q

how does meiosis contribute to genetic variation?

A
  • crossing over - genes exchange between homologous chromosomes
  • independent assortment -combinations of maternal and paternal chromosomes are aligned in metaphase
  • random segregation - random separation of maternal and paternal
    chromosomes in anaphase
35
Q

How does fertilisation contribute to genetic variation?

A
  • fusion of two gametes –> zygote with distinct allele combination.
  • many possible gamete pairings –> gene combinations –> variation
36
Q

How do mutations contribute to genetic variation?

A
  • change in the DNA sequence of a gene.
  • creates new alleles with altered gene expression.
  • if passed to offspring –> new allele in population.
  • diversity to gene pool –> increased allele frequency and population variation.
37
Q

what’s co-dominance?

A

where both alleles inherited from homozygous parents are expressed in the heterozygous offspring

38
Q

what is incomplete dominance?

A

where the alleles of homozygous parents are expressed as a blend in the heterozygous offspring

39
Q

what are multiple alleles

A

when there is more than 2 possible alleles within in a population

40
Q

what type of trait is it if both parents aren’t affected but an offspring is affected?

A

autosomal recessive

41
Q

what type of trait is it if both parents are affected and an offspring is unaffected

A

autosomal dominant

42
Q

what type of trait is it if affected mother passes on the X-linked trait to the sons(s) but not to daughter(s)

A

sex-linked recessive

43
Q

What type of trait is it if:
a) Affected father passes on the X-linked trait to the daughter(s) but not to son(s).
b) Affected mother passes on the X-linked trait to both her daughter(s) and son(s).

A

sex-linked dominant

44
Q

what is a gene pool?

A

total of all the genes and their alleles within a population

45
Q

what is genetic diversity?

A

total of all the characteristics in the genetic makeup of a species

46
Q

what does the process of DNA sequencing?

A
  1. DNA isolated and replicated.
  2. DNA denatured using heat, separated into single strands (template, complementary strand)
  3. a primer binds to the start of the template strand, helps DNA polymerase start replication process.
  4. DNA polymerase uses single DNA strand build the complementary strand of DNA using nucleotides.
  5. The complementary strand will continue until chain-terminating nucleotide is reached, which prevents any further nucleotides from attaching.
  6. terminator molecules are labelled with a different fluorescent dye depends on nucleotide base at the end of the chain.
  7. dye labelled DNA strands are electrophoresed and passed through a laser beam.
47
Q

what does the process of DNA profiling include?

A

DNA profile shown as series of bands sections in our non-coding DNA called STRs (short tandem repeats) - repeat many times, unique to each individual.
- The number of repeats in these non-coding regions of DNA varies –> different DNA profiles.
- close relation = similar DNA profiles determines inheritance patterns on a global level+family level for paternity testing/forensics.
- Its limitations involve contaminated and ‘planted’ evidence in crime scenes.

48
Q

how are population genetics used in conservation management?

A
  • make informed decisions about protecting populations that are
    endangered/near extinction.
  • Conservation genetics looks at how genes are inherited in a population to avoid extinction
  • useful for scientists when determining current and future strategies for conservation and maintenance of biodiversity.
49
Q

how is population genetics used in disease and disorder inheritance?

A

Monogenic disease - mutation in a single gene in all cells
- Congenital disease → present at birth
- prediction of genetic susceptibility - traditionally been based on
family background and pedigree analysis.
- with genetic testing, the diagnosis of monogenic diseases and probability of inheritance in future offspring quick+accurate
- Genetic testing - presence of the SNPs that are unique to a disease
can be quickly and easily through DNA sequencing.
- Large-scale screening and DNA analysis –> early detection+improved treatment options - predict inheritance of a disease/disorder.
- generating data on occurrence of specific genetic conditions

50
Q

how are population genetics related to human evolution?

A
  • our understanding of human evolution was based on fossil evidence - incomplete+subjective
  • examining the genetic variation and similarity in modern day humans –> determine origin of civilisation + evolutionary pathway.
  • evolutionary forces of mutation, natural selection, genetic drift, gene flow —> patterns of diversity in human populations today.
  • number+frequency of alleles in a population are measures of diversity.
51
Q

what’s the multi-regional hypothesis and what does it suggest?

A

Multi-regional hypothesis (MRE) suggests that Homo sapiens evolved from ‘homo erectus’ outside of Africa.
- Homo erectus wandered out of Africa –> inhabited other regions –> evolved into modern humans.
- Modern genetic studies: if MRE were correct –> modern populations have ancient alleles over different regions of the world.

52
Q

what does the out-of-Africa hypothesis suggest?

A
  • Modern humans (Homo sapiens) evolved in Africa 200,000 years ago~
  • 60,000–80,000 years ago~ a group migrated out of Africa.
  • Migrants spread across Europe, Asia, and other regions, replacing local hominins (e.g., Neanderthals).
  • Supported by genetic, fossil, archaeological evidence.
  • Higher genetic diversity in African populations –> all humans link to African ancestry.