Unit 5a Flashcards

1
Q

Bodies have 2 types of cells ____________ which are ___________ and ___________ which are _________.

A

somatic cells, body cells, gametes, sex cells

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2
Q

Somatic cells are _________ whereas gametes are _________

A

diploid, haploid

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3
Q

diploid = _____________

A

2 full sets of chromosomes

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4
Q

homologous means same gene but different ________. There are two types of chromosomes: 1-22 are ____________ and the 23rd is ____________

A

allies, autosomal, sex

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5
Q

sperm + egg = ___________. Ploidy = _____________. Duplicated chromosomes look like _______ and unduplicated look like _______.

A

zygote, number of chromosomes, X, I

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6
Q

Sister chromatids (X) went through ___________. Before Meiosis I _______________ has happened in the cell cycle. Meiosis happens ________.

A

s phase, g1, g2, interphase, twice

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7
Q

The result of meiosis is that one diploid cell becomes _______________.

A

4 haploid

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8
Q

homologous - __________________. A __________ is the chemical factor that determines traits. A _______ crosses one trait which creates a _________.

A

each of the 4 chromosomes from male parent has a corresponding chromosomes from the female parent, gene, monohybrid cross

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9
Q

A ________ crosses 2 traits. The dominant trait always takes over recessive.

A

dihybrid cross

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10
Q

Meiosis is __________________.

A

the process of reduction divisions where the number of chromosomes is cut in half through the separation of homologous chromosomes in a diploid cell

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11
Q

Prior to meiosis - cells undergo DNA replication forming duplicate chromosomes in the _____________.

A

S phase

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12
Q

What happens in prophase 1 in meiosis?

A

nuclear membrane breaks down
centrioles separate and make spindle fibers
Homologous chromosomes PAIR up and become visible
creates a tetrad
CROSSING OVER occurs

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13
Q

A tetrad is _____________. During prophase 1 crossing over occurs which is ________________.

A

cluster of 4 chromatids, exchange portions of chromatids; exchange of alleles

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14
Q

What happens in metaphase 1 in meiosis?

A

homologous chromosomes are lined up in the middle of the cell in PAIRS

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15
Q

What happens in anaphase 1?

A

pairs separate; one chromosome (2 sister chromatids) are pulled away to each side

sister chromatids stay attached

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16
Q

What happens during telophase 1 and cytokinesis during meiosis

A

chromosome gather at the poles

nuclear membrane MAY reform

cytoplasm divides into 2 cells

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17
Q

What is the result of meiosis 1?

A

2 haploid daughter cells that still have the duplicated chromosomes and are different from original diploid cells

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18
Q

What happens in prophase II of meiosis?

A

nuclear membrane brakes down

spindle fibers form AND ATTACH to the centromeres of the sister chromatids

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19
Q

What happens in Metaphase II of meiosis?

A

sister chromatids line up in the middle

20
Q

What happens in anaphase II of meiosis?

A

sister chromatids separate and are pulled away

21
Q

What happens in telophase II and cytokinesis in meiosis?

A

nuclear membrane reforms

spindle fibers disappear

cytoplasm divides

22
Q

What is the result of meiosis II?

A

4 haploid, genetically unique, daughter cells. They each have an unduplicated chromosomes/chromatid

23
Q

________ restores the diploid number. In females the cell divisions at the end of meiosis I and meiosis II are uneven so the ___________ receives the most cytoplasm. The other three bodies are known as __________ and usually do not participate in reproduction

A

fertilization, egg, polar bodies

24
Q

genes that __________ do not influence each other’s ________.

A

segregate independently, inheritance

25
What is the principles of independence assortment?
genes for different traits can SEGREGATE INDEPENDENTLY during the formation of gamete. Independent assortment helps account for the many genetic variations observed in plants, animals, and other organisms
26
__________ is where one allele is not completely dominant over another. The ___________ phenotype is a mix of the two homozygous phenotypes.
incomplete dominance, heterozygous
27
__________ is where both alleles contribute to the phenotype. ROUGH MIXTURE NOT EVENLY BLENDED .
codominance
28
______________ is where genes have more than 2 alleles. C > C^ch > C^h>C
multiple alleles
29
What is an examples of the law of independent assortment?
being tall does not affect eye color
30
Blood types are an example of ____________ and ___________ --------- Blood type AB is fully A and fully B ----------- Alleles I^a, I^b, i
codominance, multiple alleles
31
What are the genotypes? O A B AB
ii I^AI^A or I^Ai I^BI^B or I^Bi I^AI^B
32
What are the antigen and antibodies? O A B AB
none, Anti A and Anti B A, anti B B, anti A A and B, none
33
read notes on blood types
read
34
a _________ is a picture of the chromosomes arranged in pairs.
karyotype
35
Sex chromosome determine an individual's sex: Females = ________ Males = ___________ The ______ chromosome is larger than the _________.
XX, XY, X, Y
36
All human ________ carry a single X chromosome (23, X). HALF of all __________ carry X and half carry y. Half zygotes will be 46,XX and 46,XY
egg cells, sperm cells
37
Autosomal recessive disorder _______________. Read notes on disorders.
recessive genes on the autosomal chromosome cause the disease
38
________ are genes found on sex chromosomes. Males have just one X chromosomes, thus ______ X linked alleles are expressed in males even if they are ________. For Females there must be _______ of the alleles to be expressed. X^nY - __________, XY - not affected X^nX^n - __________ X^HX^h - _______
sex linked genes, all, recessive, 2, affected, affected, not affected
39
Read notes on disorders
read
40
________ shows the relationship within the family to track a trait.
Pedigree
41
What is autosomal recessive inheritance?
individuals expressing a trait has 2 normal parents two affected parents cannot have an unaffected child.
42
What is Autosomal dominant inheritance?
every affected has at least one affected parent each generation will have affect individuals
43
What is sex linked recessive?
no father to son transmission predominantly males affected trait may skip generations
44
46,XX = _______ 46, XY = ______
females, males
45
sickle cell is caused by _____________. colorblindness and hemophilia is an ____________ genetic disorder. X linked recessive is more common in _____________ when men pass X linked to daughter the daughter's son may have it (skips _____________)
codominant alleles, x linked, males, generations
46
nondisjunction is __________________
homologous chromosomes fail to separate evenly
47
45,X = ____________ 47,XXY = ___________
turners, klinefelters