Genetics Flashcards

1
Q

what is a chromosome?

A
  • consists of DNA and protein
  • human autosomal cells (somatic cells) - diploid
  • gametes - haploid
  • 23 different chromosomes
  • – somatic cells - 2 copies of 1-22 and XX or XY (diploid)
  • – gametes - 1 copy of 1-22 and X or Y (haploid)
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2
Q

the sex chromosomes

A

male - heterogametic - XY

female - homogametic - XX

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3
Q

genotype vs phenotype

A
  • genotype is the allele configurations in the DNA (D,d)

- phenotype is the characteristics displayed

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4
Q

X inactivation

A
  • one of the copies or the X chromosome in females is inactivated
  • occurs in early embryonic life
  • silenced by it being highly compacted so that it has heterochromatin
  • forms barr bodies
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5
Q

The cell cycle

A
G1 phase
- carries out normal metabolism
S phase
- DNA replication and chromosome duplication
- replication or each chromosome yeilds 2 identical chromatids 
G2 phase
- cell prepares for mitosis
M phase
- mitosis
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6
Q

stages of mitosis

A

Prophase
- chromatid fibres more tightly coiled, condensing into a tight chromosome
- formation of mitotic spindle
Prometaphase
- nuclear membrane broken down
- sister chromatids attach to u-tubules
Metaphase
- chromosomes align in the spindle
Anaphase
- sister chromatids separate to the poles
Telophase
- chromatids cluster at poles
- two daughter nuclei form around clusters
- cytokinesis then causes the division of the cytoplasm to for two daughter cells (each with 46 chromatids) (exactly the same as initial cell except chromatids not paired)

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7
Q

stages of meiosis I

A
Prophase I
- homologous paris of chromosomes associate and align
- chiasmata form (X shape)
- spindles formed
- u-tubule attaches to kinetochorse
Metaphase I
- chromosomes align in the spindle
Anaphase I
- chromosomes separate towards poles
- homologues separated
Telophase I
- chromosomes cluster at poles
- nuclear membrane formed and cytokinesis occurs
- 2 haploid cells formed (with 23 chromosomes)
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8
Q

stages of meiosis II

A
Prophase II
- spindle formed
Metaphase II
- chromosomes align in spindle
Anaphase II
- chromosomes seperate and into chromatids and move towards poles
Telophase II
- chromatids cluster at poles
- nuclei form and cytokinesis occurs
- 2 haploid cells created (with 23 chromatids)
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9
Q

non-disjunction in meiosis

A
  • incorrect separation of chromosomes or chromatids in meiosis I or meiosis II
  • leads to aneuploidy
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10
Q

down syndrome

A
  • incorrect separation of chromosome 21
  • characteristic phenotype
  • – poor muscle tone
  • – mental retardation
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11
Q

Klinefelter syndrome

A
  • incorrect separation of XY chromosome

- has both female and male traits

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12
Q

three stages of gene to protein

A
DNA (gene)
--- TXN
mRNA
--- splicing and processing
Mature mRNA
--- TLN
Protein
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13
Q

Transcriptional-level control of gene expression

A

Promoters
- additional proteins (TF’s) influence RNA polymerase binding and action (eg. TATA Box)
- TF’s are responsible for physiological change
- can either have a negative or positive effect
Enhancer regions
- sites on the DNA
- loop DNA to bring a specific promoter to the initiation complex

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14
Q

Translational-level control of gene expression

A

Hairpin

  • structures that allow mRNA to twist tightly
  • will hinder the ability for a ribosome to attach to mRNA as they are quite large
  • can also be a binding sight for an interactive protein that will influence the ribosome
  • however these structures will allow mRNA to live longer in the body
  • eg: IRE with an IRP
  • – attach to a hairpin
  • – when enough iron attaches to IRP it leaves
  • – the ribosomes can attach
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15
Q

DNA mutations

A
Processing errors
- mistakes by topoisomerase
- errors in DNA replication
DNA damage
- deamination
--- removal of amino group
--- happens often but is stopped
- depurination
--- incorrect base can be added to DNA
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16
Q

Types of mutations in the coding region

A

synonymous - no change - can create a codon that is rarely seen therefore slow for tRNA to produce it (condon bias)
non-synonymous - different amino acid
nonsense - create STOP instruction
frameshift - removing/adding nucleotide

17
Q

types of mutation in non-coding regions

A
  • promoter and enhancer regions
  • 5’ and 3’ untranslated regions
  • introns
18
Q

Autosomal dominance

A
  • mutant allele will causes disease or prevent other allele function
  • only one dominant allele required to give disease
19
Q

Autosomal recessive

A
  • often mutation equates to loss of function

- need to have 2 recessive to show disease

20
Q

X-linked dominant/recessive

A
  • special consideration as male only have one X chromosome
  • if mutant allele, you have to use it
  • effected fathers never pass to son as they get the fathers Y and mothers X
21
Q

SOME CAVEATS (exceptions)

A

germline mosaicism
- mutation arises during development - germ cells mutant
reduced penetrance
- disease causing genotype but no symptoms
age-dependent penetrance
- symptoms take lengthy time to rise (huntington’s)