Chromosomal basis of inheritance Flashcards

1
Q

What is a wild type phenotype?

A

The normal character phenotype

alternative traits are called mutant phenotypes

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2
Q

What are linked genes?

A

Genes that are located on the same chromosome that tend to be inherited together due to close proximity to eachother

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3
Q

What is unique about linked genes?

A

They do not assort independantly

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4
Q

What are incomplete linkages

A

the result of crossing over in meiosis, which exchanges segments of DNA. Recombinant phenotypes

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5
Q

What are examples of sex determining systems?

A

X-Y system for humans
X-O system for crickets
Z-W system for chickens
Haplo-diploid system in flies

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6
Q

what is a sex-linked gene?

A

a gene that is located on a sex chromosome. for humans this gene would be on the X chomosome (shared by both male and female)
fathers pass sex linked alleles to daughters, but not sons
mother pass sex-linked alleles to both sons and daughters

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7
Q

are males or females more likely to inherit sex-linked recessive disorders?

A

males. because they have only one X chromosome, any recessive allele from the mother will express the trait

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8
Q

What are examples of sex-linked disorders

A

Duchenne muscular dystrophy ( absense of X-linked gene for a muscle protein called dystrophin)
Hemophilia- (absense of one or more clotting factors)

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9
Q

What is non-disjunction?

A

When pairs of homologous chromosomes do not separate normally during meiosis.
Gametes then contain two copies or no copies of a particular chromosome

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10
Q

What is aneuploidy?

A

Occurence of extra or missing chromosomes leading to an unbalanced chromosome complement

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11
Q

What is an example of aneuploidy?

A
Down syndrome- due to 3 copies of chromosome 21 (autosomal) 
Klinefelters (XXY Male)
Turner syndrome (XO Female)
Trisomy X (XXX)
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12
Q

What are structural alterations?

A

Breakage of a chromosome the lead to changes in chromosome structure and cause human disorders
Deletion, Duplication, inversion, translocation

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13
Q

What is Deletion?

A

When a chromosome fragment lacjing a centromere is lost during cell division

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14
Q

What is duplication?

A

When a fragment becomes attached as an extra segment to a siter chromatid

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15
Q

What is inversion?

A

When a fragment of chromosome reattaches to the origional chromosome but in reverse

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16
Q

What is translocation?

A

When a chromosomal fragment joins a non homologous chromosome. some are reciprocal, some are not

17
Q

What is an example of structural alterations?

A

Cri du Chat

Specific deletion of chromosome 5. undeveloped larynx creates a high pitched cry sounding like a distressed cat.