exam 1:mendelian inheritance Flashcards

1
Q

what is genetics?

A

the science of heredity

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2
Q

what is heredity?

A

the passing of biological, genetic info (DNA) to offspring

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3
Q

what type of “ploid” are humans

A

diploid (2 sets of chromosomes)
-1 set from mom
-1 set from dad

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4
Q

how do the chromosomes become gametes

A

SPLIT–> one set of chromosomes goes to one gamete & the other set goes to the other gamete
(1 from mom and 1 from dad)

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5
Q

what bond holds the 4 DNA bases tgt

A

hydrogen bond
-not a type of covalent bond
-held tgt by electronegativity (opposite charges)

G-C (3 hydrogen bonds)
A-T (2 hygrogen bonds)

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6
Q

what type of gene makes up the majority of the genome?

A

non-coding gene

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7
Q

gene/locus

A

specific region of DNA
(may or may not code for polypeptide)

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8
Q

where are the genes/loci located

A

on chromosomes

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9
Q

what is a genome

A

all chromosomes within a cell

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10
Q

the order of DNA nomenclature

A

gene/locus–>chromosomes–>genome

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11
Q

what is the central dogma

A

DNA replication—> DNA

DNA —-transcription—>RNA—translation—> Protein

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12
Q

how are amino acids codes for

A

by triplets of DNA/ codon of DNA nucleotides (transcribed to RNA)

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13
Q

what are polypeptides made up

A

string of amino acids
-held tgt by peptide bonds

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14
Q

what are proteins made up of

A

one/more polypeptides folded tgt (3D structure)

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15
Q

why do shapes of proteins matter

A

determine the function

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16
Q

what part of aa that drives its function

A

the r-groups (how polypeptides folds)

17
Q

facts abt proteins

A

-drives biological functions in all living organisms
-DNA codes for polypeptides which form proteins
-SO, DNA= instructions for biological function (blueprint of life)

18
Q

“junk” DNA vs coding DNA

A

-theres no junk dna, they are non-coding DNA

-coding DNA: coding DNA, gets into proteins (transcribes+ translated)

19
Q

*What’s the important of having both DNA and RNA?

A

1.having both allows for genetic amplification
-making multiple copies of a gene

2.stability:
-RNA unstable, mutates easily (have 2 OHs groups)
-DNA stable, only 1 Oh group

20
Q

central dogma

A

DNA —transcription—->RNA—-translation—>protein

all living things follow it
->suggest we are evolved from a common ancestor

21
Q

all living things only have 4 nucleotides, 20 aa’s, and evolved from the single ancestor, how is there diversity

A

genome evolution
-increase the complexity of gene due to gene dupilcation=
as long there are multiple copies and a gene and those genes continue to serve a purpose, mutations are likely to occur
-gene rearrangements where the genes are similar but have differnt products

22
Q

where duplication occur for genome evolution? how do they interact?

A

occurs in
1: errors in DNA replication
2. uneven crossing over during meiosis (recombinant: homologs chromosomes-> equal and opposite)

interact by crossing over

23
Q

what did gregor mendel studied and why?

A

he use pea plants and predict specific physical features passed from parents to offspring

why? bc he wanted to increase yield of the pos traits and avoid the neg

24
Q

what was gregor mendel’s greastest contribution?

A

discovered a predictable pattern of inheritance based on random (what offspring would look like based on the parents) assortment of “genetic particles” (genes)

25
Q

artificial selection

A

based on humans selection where organisms w/ undesirable traits are killed and bred those with desireable traits

26
Q

misconceptions of inheritance

A
  1. one parent contributed more than the other to the offspring (unequal contribution)
    -did reciprocal crosses to dispell myth
  2. parental traits blended tgt in offspring and were permanently changed
    “blending inheritance”’
27
Q

why did mendel work with peas

A
  1. easy to grow
  2. easy to control fertilizations
  3. easy to produce and screen large numbers of offspring quickly
    *traits are “mutually exclusive”-“either/or”traits (cant be both)
    unlikely continuously varible:everything in between
28
Q

what does true breeding mean

A

when self fertilized, parents always produce offspring look exactly like themselves
homologous for the trait

29
Q

*mendel 1st law: law of segregation

A

during gamete formation,
a pair of alleles from each parent separate and give the offspring one alle

*def:
-2 alleles for each trait separate when gametes are formed (only 1 alle is contained in each gamete)
-alleles reunite at random- 1 from each parent via fertilization

30
Q

mendels crosses predict phenotype, how can you tell their genotypes

A

test cross

31
Q

*mendel’s 2 law: law of independent assortment

A

during gamete formation, diff pairs of alleles separate (assort) independenly
-presence of 1 specific allele does not affect presence of another

32
Q

the different between mendels 1st and 2nd law

A
33
Q

what is mendelian inheriance

A

1 gene control 1 trait

34
Q

how to we follow the pattern of inheritane( like diseases) in humanss

A

pedigree analysis

35
Q

pattern of inheritance: recessive

A

2 unaffected parents, one or more affected child
-this means that the homozygous recessive genotypes have the “disease”

36
Q

pattern of inheritance: dominant

A

2 affected parents, at least one unaffected child
-this means that the ones that is affceted are homozygous recessive