Lecture 12 Flashcards

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1
Q

what are genes

A

a segment of DNA that influences the structure & function of an organism by encoding & directing the synthesis of mRNA, tRNA, rRNA & ultimately a polypeptide

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2
Q

allele ?

A

One of two or more variants of a gene pair that occur at the same locus. A diploid individual inherits two alleles for each gene, one from each parent
Alleles can be dominant, recessive, co-dominant, or show incomplete dominance.

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3
Q

genotype?

A

We call the allelic composition of an individual, the genotype

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4
Q

phenotype?

A

the appearance, or the characteristics, the phenotype.

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5
Q

how many gens do humans have ?

A

somewhere between 21,000-25,000

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6
Q

genome?

A

The complete complement of an organisms’ genes and non-gene DNA ie all the DNA in an organism.

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7
Q

correct order of organization of genetic material, from largest to smallest?

A

Genome, chromosome, DNA, gene, nucleotide

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8
Q

how did Mendel figure out genetics

A

Lots of pea plants & math

Nothing was known about meiosis
& genes weren’t even discovered yet!

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9
Q

how did Mendel do the crossings

A

P generation: were always true breeders

Parent x Parent → F1 generation

F1 x F1 → F2 generation Crossed F1 with itself to get the F2 generation

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10
Q

Mendel’s model of inheritance

A
  1. There are alternate versions of genes (alleles)
  2. For each character: an organism inherits 2 alleles, 1 from each parent
  3. If the 2 alleles at a locus differ: the dominant allele determines the organism’s appearance
  4. 2 alleles separate (segregate) during meiosis & end up in different gametes ie each parent passes on 1 copy (not 2) of each allele.
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11
Q

Recall the life cycle

A

adult → meiosis → sperm or egg → fertilization → mitosis → embryo → mitosis → fetus → mitosis → child to adult.

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12
Q

Character?

A

A feature that can be inherited. Ex hair color

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13
Q

Trait?

A

A specific version of a character. Ex RED hair

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14
Q

_ are to genes as traits are to alleles.

A

Characters

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15
Q

Gene locus

A

a specific place along the chromosome where a given gene is located. Genes are arranged in a fixed order along the chromosome

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16
Q

Autosomes

A

The chromosomes other than the sex chromosomes

17
Q

Homologous chromosomes

A

a pair of chromosomes that carry genes for the same characters at corresponding loci. The alleles at each locus may be the same or different

18
Q

Dominant allele

A

an allele of a gene whose expression is observable in a heterozygote. ; the phenotype of the heterozygote (ex Tt) is indistinguishable from that of the dominant homozygote (TT).

19
Q

Recessive allele

A

an allele whose expression is observable only in the homozygous form (tt), ie when the dominant allele is absent.

20
Q

Law of independent assortment

A

Mendel’s second law holds that during gamete formation, genes for different traits are separated from each other independently during meiosis
random line up of chromosomes during metaphase I which results in each member of a pair of homologous chromosomes separating independently of the other chromosomes during anaphase

21
Q

Mendel discovered the Law of independent assortment based on the analysis of his ___.

A

dihybrid crosses

22
Q

Law of segregation?

A

a diploid organism passes a randomly selected allele for a trait to its offspring, such that the offspring receives one allele from each parent.

23
Q

Mendel discovered the Law of segregation based on the analysis of his __

A

monohybrid crosses.

24
Q

Monohybrid cross

A

cross parents that are true-breeders (homozygous) for the character you’re studying that differ at 1 locus

25
Q

ratio of Monohybrid cross?

A

3:1

26
Q

dihybrid cross?

A

study of inheritance patterns for organisms differing in two traits of interest.

27
Q

ratio Dihybrid cross

A

9:3:3:1

28
Q

Punnett square?

A

a diagram that is used to predict the probable outcome of a particular genetic cross. The diagram is used to determine the probability of an offspring having a particular genotype.

29
Q

Carrier

A

An individual who has a recessive, disease-causing allele at a particular locus on one chromosome of a pair and a normal allele at that locus on the other chromosome (ex if N=normal, n=disease then a carrier would be Nn) AND this individual is phenotypically normal

30
Q

which one is more specific? trait or character?

A

trait

31
Q

what % of dna is genes

A

les than 2%

32
Q

True breeders?

A

Homozygous for a specific character

33
Q

3 possible genotypes

A

Homozygous dominant: YY

Homozygous recessive: yy

Heterozygous: Yy

34
Q

Monohybrids criteria

A

(1) One character
(2) homozygous (AA or aa)
(3) 2 parents must differ (AA x aa, not AA x AA)

35
Q

Albinism: A _____ disorder

A

recessive

36
Q

Huntington’s disease: A _____ disorder

A

dominant

37
Q

Achondroplasia: a __trait

A

dominant

38
Q

do one of the parents must have the disorder if it is dominant?

A

yes.

39
Q

do one of the parents must have the disorder if it is recessive?

A

no, they can be heterozygote.