Topic 12.2: Inheritance Flashcards

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1
Q

what are the different types of inheritance

A

mendelian/monogenic = one gene
mitochondrial
polygenic = many genes
complex or multifactorial = genes + environment

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2
Q

what kind of environment can affect genotype and phenotype

A
radiation
chemicals
mutagens
diet
lifestyle
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3
Q

what are the two ways phenotype can be affected

A

genotype and environment

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4
Q

what are examples of genotype that affects phenotype

A

cystic fibrosis

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5
Q

what are examples of environment that affects phenotype

A

infection

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6
Q

what are examples of genotype and environmental factors that affects phenotype

A

diabetes
cancer
heart disease

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7
Q

what are some features of autosomal recessive individuals

A

heterozygotes unaffected ( as for recessive needs both alleles of the gene to be present for it to have an effect in an individual), so the affected individuals must be homozygous recessive
two affected individuals will only have affected offspring
two heterozygotes (carriers) have 25% chance of having affected offspring
males and females are equally affected as its on an autosome not sex linked
disease ‘comes out of nowhere’
disease can skip generations

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8
Q

what are some features of autosomal dominant individuals

A

heterozygotes affected ( as only need one allele to inherit to have an effect in an individual)
autosomal dominant diseases rarely found in homozygous state, so assume heterozygous
every affected individual (so heterozygous as that is disease) has 50% chance of having affected offspring
males and females equally affected
every affected individual will have at least one affected parent so cannot skip a generation

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9
Q

what is an example of a disease that has autosomal dominant inheritence

A

huntington’s disease

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10
Q

what is an example of a disease that has autosomal recessive inheritence

A

CF

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11
Q

what are some features of X linked recessive individuals

A

males and females unequally affected - males more
every affected (hemizygous =genes on X chromosome) male will have at least a heterozygous carrier mother to give X chromosome to son as Y is from dad
every affected female will have an affected father and a carrier mother (one from mum, one from dad)
affected males will have at least heterozygous daughters (male gives affected X chromosome to daughters, so must have at least one allele)

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12
Q

what is an example of a disease that has x linked recessive inheritence

A

haemophilia A

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13
Q

what are some features of X linked dominant individuals

A

females more likely to be affected
hemizygous males and heterozygous females affected
heterozygous affected females have 50% chance of having affected offspring
affected males cannot give trait to sons as males give Y chromosome to sons but will give to all daughters and they will all be affected

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14
Q

what are some features of Y linked recessive individuals

A

only males affected
affected males give traits to all their sons
diseases linked to maleness

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15
Q

what are some features of mitochondrial inhertied individuals

A

all individuals will inherit from their mother (egg has lots more mitochondria than sperm, and sperm mitochondria not enter egg)
mother affected = all children affected
mither unaffected = all children unaffected

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16
Q

what are some features of polygenic inherited individuals

A

more than one gene can be involved in producing a phenotype
genes on the same chromosomes are said to be linked
genes on different chromosomes are not linked
linked genes do not show independent assortment at meiosis because genes on same chromosome so alleles travel together in meiosis (so not a 1:1:1:1 ratio as more likely to not bother crossing over)
so recombination frequency (amount of crossing over) between two linked genes is dependent on distance between the genes, more DNA in between more chance of crossing over taking place as otherwise too close together = tightly linked, linked genes that are far apart on same chromosome = like unlinked genes and lots of crossing over

17
Q

what is an example of a condition involving polygenic inhertince in recessive manner

A

albinism
one of two genes involved in pathway is not working properly but both alleles of that gene affected - for both parents that have albinism, but child is heterozygous so unaffected