Gametogenesis Flashcards

1
Q

What is the three fold importance of meiosis?

A

1) Crossing over shuffles genes to provide recombination of gene material
2) Haploid gametes are produced, retaining a constancy of chromosomenumber
3) Random assortment of maternal and paternal chromosomes

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2
Q

When does the first meiotic division occur in oogenesis?

A

Not until puberty is reached and OVULATION occurs

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3
Q

At what age is there a peak number of 7 million primary oocytes?

A

5-month fetal age (ie before birth)

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4
Q

In Oogenesis, when does the oocye become halted in meiosis II?

What cell type is halted and at what phase in meiosis II is it halted at?

A

The SECONDARY OOCYTE becomes halted in METAPHASE II at OVULATION (after puberty obviously)

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5
Q

When is the PRIMARY oocyte halted in meiosis I and at what stage?

A

Before birth it is halted in Prophase I at which point it is in the dictyotene stage

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6
Q

What is the result cell type for oogenesis?

A

One oocyte and 3 polar bodies

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7
Q

What are the 5/6 cell types for speratogenesis?

What are the processes in b/w each?

A

Spermatogonia (A ->B) (via multiple mitotic divisions)

Primary spermatocytes formed when B divides

Secondary spermatocytes formed via meiosis I

Spermatids formed via meiosis II

Spermatozoa (ie sperm) formed via SPERMIOGENESIS

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8
Q

How long does it take to go from spermatogonia form to spermatozoa form?

A

64 days

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9
Q

When does the ooccye complete Meiosis II?

A

At fertilization

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10
Q

What are the layers of the oocyte?

A

Surrounded by zona pellucida and follicular cells (AKA corona radiata)

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11
Q

What are the 4 morphological changes that take place for the maturation of a sperm cell?

A

1) Most of cytoplasm is shed
2) Formation of neck, middle piece, and tail
3) condensation of nucleus
4) Fomation of acrosome, containing enzymes needed to penetrate egg

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12
Q

Where do sperm go following spermiogenesis?

A

They enter the lumen of the seminiferous tubules in the testis, and will be stored in the EPIDIDYMUS.

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13
Q

What are the 2 main types of chromosomal abnormalitites?

A

Numerical and Structural

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14
Q

What is the main cause of numerical chromosomal abnormalities?

A

Nondisjunction

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15
Q

What is aneuploidy and what is polyploidy?

What are the principle causes?

A

Aneuploidy: Deviation from the chromosome # that is NOT multiple of the haploid # of 23 (eg trisomy or monosomy). Principle cause: nondisjunction

Polyploidy: deviation from chromosome # that is a multiple of the haploid # (eg triploidy which is 69 chromosomes). Principle cause: dispermy (when an oocyte is fertilized by 2 sperm)

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16
Q

Trisomy of the autosomes is associated w/ what 3 major syndromes?

What are the main characteristics of each?

A

Trisomy 21: Down’s syndrome: flat nasal bridge, simian crease in palm of hands, eyes

Trisomy 18: Edward’s syndrome: short sternum, rocker-bottom feet, characteristic finger positioning

Trisomy 13 Patau’s syndrome: sloping forehead, malformed ears, bilater cleft lip/palate, polydactyly

17
Q

Describe 3 trisomies/monosomies of sex chromosomes and their main characteristics.

A

1) Klinefelter syndrome (XXY males): tall, small testes, sterile
2) Triple X (XXX female/XXY): usually tall, and agressive for males, 15-25% mildly retarded
3) Turner syndrome (45, XO): monosomy where female infants usually show webbed neck w/ extra skin, short stature and lack of sexual maturity

18
Q

How do structural chromosmal abnormalities usually occur?

A

Usually result from chromosome breakage (induced by environmental factors like drugs, radiation, viruses, etc)

19
Q

What is cri-du-chat and what is characteristic of it?

A

It is a structural chromosomal abnormality when a chromosome breaks and a piece of chromosome 5 is deleted.

Affected humans have a weak, cat-like cry, and severe mental retardation

20
Q

What % of malformations are caused by gene defects?

21
Q

What is genomic imprinting?

A

It is when expression of characteristics of the syndrome can be dependent upon paternal or maternal genetic material

22
Q

An example of GENOMIC IMPRINTING is when a deltion of band q12 on chromosome 15 happens.

What is it called if the deletion occurs on chromosome 15 of the 1.Mother, 2.Father?

A
  1. Mother: Angelman syndrome (AKA Happy Puppet syndrome)
  2. Father: Prader-Willi syndrome (child becomes obese)