Day 7, Lecture 2 (Aug 30): Genetics XI: Non-Mendelian Inheritance Flashcards Preview

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Flashcards in Day 7, Lecture 2 (Aug 30): Genetics XI: Non-Mendelian Inheritance Deck (13)
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1
Q

Mono-allelic expression

A
  • about 100 genes are imprinted
  • of these 100 genes only one allele is acitve, while the other allele is inacitve (imprinted/silenced)
  • Which allele is imprinted/silenced is determined by parent-of-origin
    • since only one copy is active:
      • there is limited redundancy- if the active copy has a problem, the other allele cannot correct
      • The pedigree in such cases can be quite confusing
2
Q

Silencing/imprinting is an epigeneitc phenomenon, as it is not caused by

A

changes to the DNA itslef, but due to differential methylation of cytosines

3
Q

Uniparental disomy

A
  • a unique situation, in which an individual has inherited both copies of an allele or (part of) a chromosome from one parent, rahter than the typical situation of receiving one copy from each parent. There may be 2 consequences to this phenomenon:
    1. AR disorders with only one parent being a carrier of a ‘mutated’ allele associated with an AR disorder: eg. about 1/500 children with CF have CF due to homozygous mutations in CFTR, both copies inherited from mother- this is called uniparental isodisomy
    2. Disorders of imprinting: an example is Prader-Willi syndrome, in which you need the paternal chr 15 but it is not presnet and the maternal is methylated
4
Q

Imprinting

A
  • Typically, the protein produced via DNA→mRNA→protein is made 50% by one allele, and 50% by other allele
    • For example, phenylalanine hydroxylase (PAH) activity is 50% in a parent of a child with severe PKU, as one allele is non-funcitonal
      • The activity is enough to not show clincal symptoms, but enzyme level/activity is not normal
  • Imprinted genes constitute about 80-100 genes (of the about 20,000 in the human genome)
  • of these 80-100 genes, only one allele is active, while the other allele is inactive (aka imprinted or silenced)
    • this is named mon-allelic expression
      • Which allele is imprinted/silenced, and which allele is active is determined by ‘parent of origin’
  • this silencing is an epigenetic phenomenon, hence is not caused by DNA changes, but due to differential allele methylation
  • in some genes
    • the silenced copy is paternal in origin
    • in other genes, the silenced copy is maternal
  • Since only one copy in imprinted genes is active
    • there is limited redundancy
      • if the active copy has a problem, the other allele cannot correct it
      • The pedigree in such cases can be quite confusing
5
Q

Which allele is imprinted/silenced, and which allele is active is determined by

A
  • ‘parent of origin’
    • during gametogeneiss the parental/maternal imprints are ‘wiped off’, and the paternal/maternal imprint is placed.
6
Q
A
7
Q

Imprinting diseases may be associated with

A
  • Disorder imprinting
    • example:
      • Beckwith-Wiedemann syndrome
  • Mutation of the active allele
    • Examples:
      • Prader-Willi syndrome
      • Angelman syndrome
8
Q

Beckwith-Wiedemann syndrome (BWS)

A
  • example of Disordered imprinting
  • Recognizable mutli-system with:
    • Macrosomia (large infant)
    • Macroglossia (large tongue)
    • Omphalocele
    • Tendency to hypoglycemia
    • Unusual ear-pits
  • Genetics:
    • 50-60% of BWS are due to a problem in the gene LIT1 in the Beckwith-Wiedemann critical region
      • normally, the maternal copy of LIT1 is imprinted (silenced), while paternal copy active)
      • if maternal LIT1 is hypo-methylated, both copies are active, and cause BWS
    • 2-7% of BWS cases are due to a problem in the gene H19, in the BWS critical region
      • Normally, the paternal copy of H19 is imprinted (silenced), while maternalcopy is active
      • If maternal H19 is hyper-methylated, both copies are in-active, and cause BWS
    • 10-20% of cases are caused by uniparental disomy
    • 5-10% have a mutation in the gene CDKN1C, another imprinted gnee in the BWS critical region
  • Cases of IVF and ICSI (intra-cytoplasmic sperm injection) the risk of BWS is increased
    • presumably, ICSI may obtain sperm that hasn’t yet properly been de-methylated and re-methylated in gametogenesis
9
Q

If a mutation is on the allele that is imprinted than

A

no disease results

10
Q

What was the first disorder described as associated with imprinting

A
  • Prader-Willi Syndrome (PWS)
    • 50-60% of pts have a deletion in the 15q11.2 region
      • if the deletion is on the paternally inherited chromosome, PWS is the consequence
        • This is because the SNRPN gene is active if paternally inherited
    • the other 40% of pts with PWS do not have a deletion
      • Some of the pts with PWS who do not have a deletion, have maternal uniparental disomy, resulting in the absence of paternally acitve SNRPN
      • one possible mechanism causing maternal uniparental disomy in PWS is ‘trisomy rescue’
11
Q

Trisomy Rescue

A
  • Uniparental disomy ussually arises due to an error in meiosis. Two chromosomes in either the egg or sperm cell fail to separate and both get passed to the fetus. As a result, the fetus inherits three chromosomes (Trisomy) rather than two. In relatively rare situations, one of the three chromosomes is lost (termed trisomy rescue), resulting in a “normal’ two chromosome state (disomic) after fertilization. one-third of the time, this loss will result in uniparental disomy
12
Q

Angelman syndrome is not usually due to ‘trisomy’ rescue, because non-dysjuntion is typically a _____ problem. However, Angelman may be due to

A
  • non-dysjunction is typically a maternal problem (esp. in Meiosis I)
  • However, angelman may be due to ‘monosomy’ rescue
13
Q

What is the most common trisomy

A

16, but does not get as much attention because it results in miscarriages and not viable births

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