Inheritance Flashcards

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1
Q

What is a homologous chromosome?

A

A pair of chromosomes in diploid cells. One inherited from mother and one from father. Same size same genes but may have different alleles.

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2
Q

What are sex chromosomes

A

X and Y chromosomes

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3
Q

What are autosomes

A

Autosomes are all chromosomes except sex chromosomes

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4
Q

What is a gene

A

A gene is a specific DNA sequence that codes for polypeptide

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5
Q

What is a sex-linked genes?

A

Genes on sex chromosome

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6
Q

What is an autosomal linked genes?

A

Genes on autosomes

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7
Q

What are linked genes

A

All genes on the same chromosome. They are in a linkage group. Likely to be inherited together. (Not the same with sex/autosomal-linked genes

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8
Q

What is an allele

A

A form of gene➡️result of mutation

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9
Q

What is a locus

A

Locus plural loci is a position of gene on chromosome

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10
Q

What is a diploid cell

A

Diploid cells have two sets of chromosomes (2n)
= 2 copies of each gene = 2 alleles
1 maternal, 1 paternal
* somatic cells= all cells except for gametes
* In humans: 2n =46
➡️result of mitosis

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11
Q

What is a haploid cell

A

Haploid cells have only one set of chromosomes (n)
= only one copy of each gene = 1 allele
* gametes/germ cells
In humans n=23
➡️ result of meiosis

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12
Q

When does meiosis occur

A

Meiosis aka reduction division
Before fertilisation in sexual reproduction

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13
Q

What is the importance of meiosis

A
  • To produce gametes/sex cells with half the no. of chromosomes
  • Mantain the diploid no. of chromosomes in each generation
  • To produce genetic variation in offspring
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14
Q

Describe what happens during prophase 1 of meiosis

A
  • Condensation of chromatin/chromosome
  • Centrosomes move to opposite poles
  • Nuclear envelope breaks down
  • Nucleolus disappears
    *Spindle fibres form
    ➡️ start attaching to centromere and pull

*Synapsis occurs
➡️ Process where homologous chromosomes pair up
➡️ Each pair is called a bivalent/tetrad

*Crossing over takes place between non-sister chromatids
➡️ At chiasmata (singular: chiasma)
➡️ Results in exchange of genetic material

*During synapsis, homologous chromosomes coil around each other intimately
* Remain in contact at chiasmata
*Site of crossing over: chiasma

*Part of chromatid break
* Reconnect to another non-sister chromatic

Result in:
➡️ Exchange of genetic material (NOT genes)
➡️ Linkage groups broken/ linked genes on same chromosome are separated
➡️ New combination of alleles within each chromosome
➡️ Genetic variation

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15
Q

Describe what happens during metaphase 1 of meiosis

A
  • centrosomes reach opposite poles
  • spindle fibres are fully formed
    ➡️ attached to chromosomes at centromeres

*Bivalents/ tetrads line up across equator/ metaphase plate
➡️ chromosomes line up in pairs

*Independent assortment of homologous chromosome pair occurs
➡️ Each pair lines up independently of others on equator
➡️ e.g. could be red-blue or blue red
➡️ Results in gametes that are genetically unique

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16
Q

Describe what happens during telephase one of meiosis

A
  • chromosomes reach the poles
  • chromosomes partially decondenses
  • nucleolus reforms
  • Nuclear envelope reassembles
  • spindle fibres breakdown
  • Cytokinesis occur
  • number of chromosomes in each daughter cell are now halved
  • Two haploid cells formed
17
Q

Describe what happens during cytokinesis in meiosis and animal cell

A

Cytokinesis is the division of cells cytoplasm

In animal cells:
* cell membrane drawn together
➡️ by contractile ring of microfilaments
➡️ forms a cleavage furrow
➡️ creating a drawstring effect

  • cell membrane fuses
  • to divide cell into two
  • organelles are shared out
18
Q

Describe what happens to cytokinesis in plants during mitosis

A

In plants:
* Vesicles transported to equator
➡️ to form cell plate at equator
* cell wall laid down

  • so cytoplasm divided into two
  • Organelles are shared out
19
Q

Brief interphase between meiosis 1 and meiosis 2

A

*Called interphase ll/ interkinesis
*Growth
* Synthesis of protein and other substances
*No DNA replication

*Plant cells go straight into meiosis ll
*No reformation of nucleolus and nuclear envelope

20
Q

Describe prophase ll in meiosis

A

P/S: Meiosis is just like mitosis

*Condensation of chromatin
* Spindle fibres form
➡️ Start attaching to centromere
* Centrosomes move to opposite poles
* Nuclear envelope breaks down
* Nucleolus breaks down

21
Q

Describe metaphase ll

A

*’Centrosomes reach opposite poles
* Spindle fibres fully formed

  • Chromosomes line up at the metaphase plate/ equator
    *At right angles to first equator

*Chromosomes attached to spindle fibres at centromere/ kinetochore

*Independent assortment of sister chromatids

22
Q

Describe the anaphase ll of meiosis

A
  • Centromere of each chromosome divides
  • Sister chromatids split at the centromere

*Spindle microtubules shorten
* Chromatids move to opposite poles
➡️ With centromeres leading towards poles

23
Q

Describe telophase ll and cytokinesis of meiosis

A

*Chromatids reach the poles
*Chromosomes decondense
➡️Become long and thin

*Nucleolus reforms
*Nuclear envelope reassembles
* Spindle fibres break down

*cytokinesis occurs

➡️ 4 haploid cells formed

24
Q

How does meiosis cause genetic variation?

A
  1. crossing over at prophase one

*Between non sister chromatids of homologous chromosomes at chiasma

➡️ Exchange of genetic material (not genes)
➡️ linkage groups broken/linked genes on same chromosome are separated
➡️ new combination of alleles with an each chromosome so genetic variation

  1. Random/ independent assortment of homologous chromosomes @ metaphase l
  • each pair lines up independently of other on equator
  • Possible combinations= 2^n
    ➡️ results in gametes that are genetically unique
  1. Independent assortment of chromatids @ metaphase ll
  2. Possible chromosome mutation
    *Faulty meiosis may cause changes to chromosome number or structure ➡️ New alleles

P/S: besides meiosis, fertilisation can also cause genetic variation!
This is due to;
Random mating
Random fusion of gametes

25
Q

Define genotype

A

Genotype= the alleles possessed by an organism
Gene=a specific DNA sequence that codes for polypeptide
*Represented by same alphabet 9e.g. B and b= same gene, different allele)

Allele=a form of gene ➡️ result of mutation
*Dominant allele represented by capital letter and always placed in front 9e.h. B)
*Recessive allele represented small letter and always places behind (e.g. b)

26
Q

Define phenotype

A

Phenotype:the observable characteristics of an organism
➡️ Can be influenced by genotype, environment

27
Q

Define homozygous and heterozygous

A

Diploid cells: 2 sets of chromosomes, so 2 alleles
*Homozygous= have two identical alleles of a gene
*Can be homozygous dominant 9e.g. BB) OR homozygous recessive (e.g. bb)
*Heterozygous= have two different alleles of a gene (e.g. Bb, NEVER bB)

28
Q

Define dominant allele

A

*Expressed in the phenotype even when only one copy of the allele is present
*Expressed in heterozygotes and homozygote for the allele (e.g. Bb and BB)

29
Q

Define recessive allele

A

Expressed in the phenotype only when two copies of the allele are present
* Expressed only in a homozygote for the allele (e.g. bb)

30
Q

Describe monohybrid cross

A

*Trait is controlled by 1 gene
*Mendel crossed a purebred tall pea plant and purebred short pea plant. Both are homozygous
*This is the parental (P) generation

*All resulting offspring in the F1 generation is tall
*Crossed offspring in F1 with each other (self-fertilisation)
*In the resulting F2, he obtained 787 tall and 277 short pea plants
*Aproxx. A ratio of 3:1

We can represent genetic crosses using a genetic diagram

Every genetic diagram must have:
1)Parental phenotypes
2) Parental genotypes
3) Gametes (you must circle gametes)
4) Offspring (F1) genotype and phenotype
You MUST draw a punnet square
R) Probability/ratio
Depends on what the question wants

31
Q

What must every genetic diagram have?

A

Every genetic diagram must have:
1)Parental phenotypes
2) Parental genotypes
3) Gametes (you must circle gametes)
4) Offspring (F1) genotype and phenotype
You MUST draw a punnet square
R) Probability/ratio
Depends on what the question wants

32
Q

What is a test cross

A

Test cross= method to determine exact genotype of a dominant phenotype organism
➡️ is it homozygous dominant or heterozygous for the gene?
➡️ cross with individual homozygous recessive for the gene
➡️ also known as a short plant (TT)

If the tall plant is TT:
*TT x TT
➡️ All offspring will be tall (Tt)

If the plant is TT:
*Tt x TT
➡️ offspring can be either tall (TT) or short tt) Escape room

33
Q

Define purebred

A

A cross of same purebred organisms always produce offspring with the same genotype. Homozygous individuals

34
Q

Define parental (P) generation

A

Initial generation

35
Q

Define F1 and F2 generation

A

F1 generation: stands for first filial generation/first set of offspring
Result of crossing w different purebreds (i.e. 2 homozygotes of different phenotypes). F1 offspring are all heterozygotes

F2 generation: offspring result of self pollination of F1 plants OR cross of 2 heterozygotes

36
Q

What is a test cross

A

Test cross is a method to determine exact genotype of a dominant phenotype organism. Cross with individual homozygous recessive for the gene(s).