Unit 5 - Heredity Flashcards

1
Q

Gametes

A
  • a sex cell ( sperm or an egg)
  • designated by the n number
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2
Q

What are gametes made by?

A

meiosis

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3
Q

Gametogenesis

A

the process in which cells undergo meiosis to make sex cells

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4
Q

Haploid Number

A

n - number of chromosomes

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5
Q

Oocyte

A

egg cell

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6
Q

Fertilization

A
  • sperm and egg meet (sperm enters egg)
  • restores the diploid number (2n) bc two haploid gametes each containing half the number of chromosomes (the haploid number), combine to form a diploid.
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7
Q

Diploid

A
  • a number of chromosomes in in a body cell
  • 2n
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8
Q

Body cells

A

somatic cells - autosomes

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9
Q

autosomes

A

are the chromosomes that determine traits other than sex (e.g., eye color, height, metabolism).

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10
Q

Somatic Cells

A

are all the cells in your body except gametes (sperm and egg cells).

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11
Q

Karyotype

A

picture of the chromosomes

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12
Q

Homologous Chromosomes

A

separate chromosomes (NOT DUPLICATED CHROMOSOMES) that code for the same type of genes (ex. height )
- inherited

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13
Q

Mitosis

A

produces 2 genetically identical cells

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14
Q

Meiosis

A

produces gametes ( provides variety )

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15
Q

Interphase (part of S-phase)

A
  • start with 6 chromosomes and duplicate the chromosomes
  • in the end we should have 4 haploid cells with half chromosomes in each so 3 in each
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16
Q

Meiosis 1 ( the first division )
Prophase 1

A
  • chromosomes condense
  • homologous chromosomes pair up (one from dad and one from mom)
  • recombination of genes (when they pair up they combine to make tetrad and chiasma
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16
Q

Synapsis in Prophase 1

A

when the homologous chromosomes pair up (one from dad and one from mom)

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17
Q

Tetrad in Prophase 1

A

is created when two homologous chromosomes (one from each parent) pair up.
Each chromosome in the pair has two identical sister chromatids. Together, that makes 4 chromatids total, hence the name “tetrad.”

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18
Q

Chiasma

A

physical site where homologous chromosomes overlap and swap DNA. So this is where they are touching and where they recombine to get that variety

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19
Q

Meiosis 1
Metaphase 1

A

the homologous chromosomes line up

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20
Q

Law Of Independent Assortment

A

chromosomes can line up in many different arrangements

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20
Q

Meiosis 1
Anaphase 1

A
  • homologous chromosomes separate
  • if chromosomes don’t separate correctly then you have non-disjunction which is uneven distribution of chromosomes
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20
Q

Meiosis 1
Telophase 1

A

two haploid cells are made and they are genetically different

20
Q

Why do the chromosomes go straight to prophase and not to interphase when you go to meiosis 2?

A

After Meiosis I, the sister chromatids are already present, so there’s no need to replicate the DNA again before Meiosis II.

20
Meiosis 2 Prophase 2
nuclear envelope breaks down
21
Meiosis 2 Metaphase 2
chromosomes line up
21
Meiosis 2 Anaphase 2
the sister chromatids pull apart
22
Meiosis 2 Telophase and Cytokinesis
both cells divide again, making four unique haploid cells. and now we make sex cells so 4x sperm, 1x egg, and 3x polar bodies that are useless
23
polar bodies
small non-usable cells that do not fertilize and they get reabsorbed into the body
24
Law Of Segregation
genes that go into gametes sort randomly and this allows for variety
25
Autosomal Inheritance
inherit 2 of every kind
26
Phenotype
observable characteristics so what protein is being made and expressed
27
Genotype
actual gene that codes for a protein to express phenotype
28
Allele
- different forms of a gene - ex. you receive brown hair from mom and blond hair from dad
29
How does genotype determine phenotype
genotypes code for the production of a protein and that protein gives our physical traits
30
Homozygous dominant
An individual has two dominant alleles for a gene (e.g., AA).
31
Heterozygous
An individual has one dominant allele and one recessive allele for a gene (e.g., Aa).
32
Homozygous recessive
An individual has two recessive alleles for a gene (e.g., aa).
33
Locus
specific location of a gene
34
On the genetic level what is happening?
- gene codes for a protein - gene gets transcribed into mRNA - mRNA goes to the ribosomes to make a protein
35
Homozygous dominant (true breeding)
Two dominant alleles for a trait (AA). Always passes on the dominant allele to offspring.
36
Homozygous recessive (true breeding):
Two recessive alleles for a trait (aa). Always passes on the recessive allele to offspring.
37
Heterozygous (hybrid):
One dominant and one recessive allele for a trait (Aa). Displays the dominant trait but can pass on either allele to offspring.
38
Carrier
A heterozygous individual for a recessive trait (Aa) that does not express the recessive condition but can pass the recessive allele to offspring.
39
Wild Type
the original/ natural form of a gene
40
Blood Clotting
- original form: blood clotted and clot broke down - mutated: blood clots and clots and clots
41
Phenotypic ratio
9:3:3:1
42
What happens to chromosome numbers in both meiosis 1 and meiosis 2?
The number of chromosomes in a cell is halved during meiosis I and maintained during meiosis II
43
Imcomplete Dominance
neither allele is dominant over the other so its the blending of allele resulting in a new phenotype
44
Co dominance
both alleles are expressed in the heterozygous condition
45
Polygenic Inheritance
multiple genes that will code for one specific phenotype
46
Epistasis
multiple genes that code for a phenotype and one gene that modifies/controls phenotype
47
Linked Traits
genes found on the same chromosome
48
49
Epistasis
multiple genes that code for a phenotype and one gene that modifies/controls phenotype
50
If genes are located on different chromosomes what does that mean
it means they assort independently and u expect a 1:1:1:1 ratio