Ch 10 Flashcards

1
Q

What are homologous chromosomes?

A
  • One chromosome of each pair comes from the mother and one from the father.
  • Homologous chromosomes are similar but not identical. Each carry the same genre in the same order, but each trait is not the same.
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2
Q

What are homologous pairs?

A
  • a zygote contains 1 set of chromosomes from the ovum and 1 set from the sperm
  • each set=a homologous pair of chromosomes
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3
Q

What is a gamete? 2n or n?

A

Gametes= reproduction cells = 1n cells = ovum/sperm

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4
Q

Are gametes diploid or haploid?

A

Haploid= 1n

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5
Q

How many chromosomes do human gametes have?

A

diploid number of chromosomes is 46, the haploid number is half of this, or 23 chromosomes.

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6
Q

If synapsids means joined, when are homologous chromosomes joined? Why is it called bivalent?

A

-when homologous chromosomes line up at the metaphase plate they are attached and align very closely.
Bivalent: there are two chromosomes

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7
Q

During meiosis I what lines up at the metaphase plate?

A

-homologous chromosomes line up across from one another along the metaphase plate

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8
Q

What is crossing over? During which phase of meiosis I does this occur?

A
  • During meiosis, crossing over occurs during prophase I.
  • It is the exchange of genetic material between homologous chromosomes that results in recombinant chromosomes, which contribute to genetic diversity.
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9
Q

During what phase do homologous chromosomes separate?

A

-anaphase II

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10
Q

When does interkinesis occur?

A

A short rest period to the second nuclear division occurring in meiosis II

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11
Q

What chromosomes are in the nucleus of a cell during interkinesis?

A
  • a short rest period prior to these end nuclear division occurring in meiosis II
  • chromosomes still consist of two chromatids
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12
Q

Are cells diploid or haploid during metaphase II?

A

-Haploid number of duplicated chromosomes at metaphase plate

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13
Q

During what phase do sister chromatids separate in meiosis II?

A

Anaphase II

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14
Q

How many daughter cells (gametes) are formed from one parent cell at the end of meiosis?

A

.During meiosis one cell divides twice to form four daughter cells. These four daughter cells only have half the number of chromosomes of the parent cell – they are haploid. Meiosis produces our sex cells or gametes

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15
Q

What is the process of sperm formation and maturation called?

A

Spermatogenesis
-results in four cells that become sperm
Begins with primary spermatocytes
*has 46 chromosomes
-primary spermatocytes divides meiotically to form two secondary spermatocytes
*each set with 23 duplicated chromosomes
-secondary spermatocytes divide to produce four spermatids

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16
Q

What is the process of egg formation called?

A
  • oogenesis
  • begins with primary oocytes
  • has 46 chromosomes
  • primary oocytes divided meiotically to form two secondary oocytes
  • each with 23 duplicated chromosomes
17
Q

Define euploidy.

A

-correct number of chromosomes

18
Q

What is aneuploidy?

A

-changes to euploid: aneuploidy
-aneuploidy: monosomy and trisomy
*monosomy: an individual has only one of a particular type of chromosome
*trisomy: an individual has three of a particular type of chromosome
Due to nondisjunction

19
Q

How does nondisjunction result in aneuploidy?

A
  • nondisjunction is the cause of abnormal chromosome numbers
  • aneuploidy: monosomy and trisomy
  • monosomy: an individual has only one of a particular type of chromosome
  • trisomy: an individual has three of a particular type of chromosome
20
Q

What disorder is caused by nondisjunction of chromosome 21?

A

Down syndrome is usually caused by an error in cell division called “nondisjunction”

21
Q

How does nondisjunction result in a female with Turner syndrome?

A
  • Genotype XO
  • have only one sex chromosome
  • affected individuals are sterile females
  • ovaries never become functional
  • do not undergo puberty
  • are short, have a broad chest, folds of skin on the back of the neck
  • otherwise normal
22
Q

How does nondisjunction result in a male with Klinefelter syndrome?

A
  • genotype. XXY
  • three sex chromosomes
  • one Y chromosome and two or more X chromosomes
  • Affected individuals are sterile males
  • testes and prostrate are underdeveloped
  • no facial hair
23
Q

What happens to a chromosome when there is a deletion?

A
  • end of a chromosome breaks off

- —or two simultaneous breaks lead to the loss of internal segment

24
Q

Are there diseases caused by deletions?

A
  • Williams syndrome

- Cri chat syndrome

25
Q

What happens to a chromosome when there is an inversion?

A

-inversion: a segment that has become separated from the chromosome in reinserted at the same place but in reverse.

26
Q

Does inversions cause disease?

A
  • inversion has occurred when a segment of a chromosome has been turned around 180°
  • Most individuals with inversions exhibit no abnormalities, but this reversed sequence of genes can result in duplications or deletions being passed on to their children
27
Q

What happens to a chromosome when there is a translocation?

A
  • segment is removed from one and inserted into another nonhomologous chromosome
  • translocation between chromosome 21 and 14
  • duplication: a chromosomal segment occurs more that once in the same chromosome.
  • inversion: a segment that has become separated from the chromosome in reinserted at the same place but in reverse.
28
Q

Are there disease caused by translocations?

A
  • Down syndrome
  • Alagille syndrome
  • certain types of cancer