Genetics Flashcards

1
Q

Genes

A

unit of genetic material, a defined portion of chromosomes that encodes for a particular trait or substance such as hair color, blood type, etc.

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2
Q

Alleles

A

the different forms a particular gene can occur in (brown, green, blue)- you have two copies of each gene (one from mom and one from dad) so there are two potential alleles for each

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3
Q

homozygous

A

2 identical alleles for a particular gene

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4
Q

heterozygous

A

2 different alleles for a particular gene

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5
Q

Dominance

A

will always be expressed, indicated by a capital letter

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6
Q

Recessive

A

will be masked by a dominant gene, can only be expressed if there is no dominant gene present- indicated by a lower case letter

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7
Q

Codominant

Incomplete dominant

A

neither masks the other so both are expressed (AB blood type)
Incomplete dominance- the traits blend (pink, RW, RR red, WW, white)

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8
Q

Genotype

A

the makeup of the genes, which 2 alleles are present

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9
Q

phenotype

A

what actually gets expressed-what you “see”

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10
Q

Monohybrid cross of dominant or recessive traits
mom brown eyes-Bb
dad blue eyes-bb

mom brown eyes-Bb
dad brown eyes-Bb

A

50% blue eyes (bb)
50% brown eyes (Bb)

75% brown eyes- BB or Bb
25% blue eyes- bb

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11
Q

dihybrid cross

A

two traits, four results or phenotypes will be seen

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12
Q

Blood Types

A

are based on what is on the cell surface
Type A- A antigen on red blood cell’s (RBCs) surface
Type B- B antigen on the surface
Type AB- both A and B antigens on the surface
Type O- neither A or B antigen on the surface

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13
Q

genetics of blood types

A

O is recessive, must be homozygous (OO)
A is dominant, can be AA or AO
B is dominant, can be BB or BO
AB is codominant

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14
Q

Blood Donation/transfusion

A

Type A-makes antibodies against B, can receive from A or O
Type B- makes antibodies against A, can receive from B or O
Type AB- can receive from everyone (A, B, or O)
Type O- makes antibodies against A and B, can only receive from O, but is a universal donor

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15
Q

Rh disease
Rh+ is dominant
Rh- is recessive

A

a situation where Rh- mother is carrying an Rh+ child. After she is exposed to Rh+ RBCs during the first pregnancy, she may produce IgG antibodies which will cross the placenta and attack fetal RBCs in later pregnancies

hemolytic disease of the newborn

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16
Q

X chromosomes disease

A

generally affects males since they only have on X chromosome, the second X chromosome is always a good back up for females

Hemophilia- x-linked disorder, recessive, defect in blood clotting protein
Color blindness

17
Q

Autosomal Recessive disorders

A
2 copies of the bad gene in order for it to be expressed 
Albinism
Sickle cell anemia
PKU
Cystic fibrosis
18
Q

Albinism

A

a defect in the production of melanin

19
Q

Sickle Cell Anemia

A

single amino acid change in the gene that makes hemoglobin, RBCs have sickle shape

20
Q

PKU

A

Phenylketonuria-enzyme defects leads to the build-up of phenylalanine in the bloodstream and neurological problems

21
Q

cystic fibrosis

A

enzyme defect causes the production of abnormal mucus that cause problems in the respiratory and gastrointestinal tract

22
Q

Chromosomal and structural disorders

A

physical or structural defects in the chromosomes rather than in the genes, often from nondisjunction- where one or more chromosomes pairs do not separate during mitosis or meiosis

Trisomy/Polyplodiys- an unusual amount of a particular chromosome
Ex: down syndrome (aka trisomy 21), XXY or XYY extra copy of a chromosome
Monosomy/anuplodiy- one copy of a chromosome, just an X, example: Turner’s syndrome

23
Q

Replication fork

A

the initial step is the splitting the two strands to form a replication fork- it involves the helicase enzymes

24
Q

DNA polymerase-

A

synthesis the DNA complementary strand

25
Q

Ligase

A

joins the gaps in the lagging DNA strands

26
Q

transcription

A

One strand of DNA molecule is read to reproduce messenger RNA (mRNA)

27
Q

Translation

A

The mRNA attaches to ribosomes to trigger the production of protein- the codons in the mRNA are “read” by transfer RNA (tRNA) to place the appropriate amino acids in their place

28
Q

Promoters

A

The DNA sequence that triggers gene expression and transcription

29
Q

Repressors

A

which block gene expression

30
Q

Operons

A

a cluster of genes controlled by a single promoter

31
Q

Mutation

A

a permanent change in the structure of the DNA, which is passed on to the offspring of the effected cells, may or may not be noticeable or harmful

Source= radiation and chemical…virusus can cause mutaitons also

32
Q

Missense

A

a single base is changed- leads to a change in the codon (UGC to UGG), which in turn leads to the production of a different amino acid, the “sense” or meaning of the codon has been changed
A change in the first two of the three letters in a codon has the grates impact

33
Q

Nonsense

A

single base change- leads to a change in the codon so that it becomes a stop codon which terminates the synthesis of the protein at that point the mRNA instead of at the real of the protein

Location of the stop codon determines its impact

34
Q

Frame-shift

A

The way the codons in the mRNA are read is messed up by adding or removing bases (location determines impact)

insertion- extra base is inserted into the DNA molecule - this throws off the codon it ends up in all those ‘downstream’ from the point (major change)

deletion- base is delated “downstream” major change

35
Q

Recombination

A

transfer of genetic information from one organism to another
donor to recipient

36
Q

Transformation

A

DNA from a dead bacteria which is broken apart is taken up through the cell wall of the recipient bacteria and integrated into its own DNA

37
Q

Conjugation

A

involves the exchange of a small piece of DNA (a plasmid) or possible chromosomal DNA from one bacteria to another-the bacteria are joined by a tube known as sex pilus

38
Q

Transduction

A

a virus (bacteriophage) carries genetic info from one bacteria to another

39
Q

Transposons

A

transposable genetic elements - also known as “jumping genes” - genetic elements that move from one pace to another within a chromosome