Mitosis versus Meiosis

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Mitosis versus Meiosis Mitosis - the division of 1 cell to produce 2 genetically identical daughter cells - diploid (2n) = contains 2 copies of the genome Meiosis - the division of 1 cell into 4 daughter cells (egg or sperm) containing ½ the genetic material - haploid (n) = contains 1 copy of the 2n 46 chrom 2n (46) 2n (46) n (23) n (23) 2n 46 chrom n 23 n 23 n 23 n 23

description

Mitosis - the division of 1 cell to produce 2 genetically identical daughter cells - diploid (2n) = contains 2 copies of the genome. Meiosis - the division of 1 cell into 4 daughter cells (egg or sperm) containing ½ the genetic material - haploid (n) = contains 1 copy of the genome. - PowerPoint PPT Presentation

Transcript of Mitosis versus Meiosis

Page 1: Mitosis versus Meiosis

Mitosis versus MeiosisMitosis

- the division of 1 cell to produce 2 genetically identical daughter cells

- diploid (2n) = contains 2 copies of the genome

Meiosis- the division of 1

cell into 4 daughter cells (egg or sperm) containing ½ the genetic material

- haploid (n) = contains 1 copy of the genome

2n46 chrom

2n(46)

2n(46)

n(23)

n(23)

2n46 chrom

n23

n23 n

23 n

23

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Development of male and female gametes

The Formation of sex cells during meiosis is referred to as gametogenesis

Sperm and egg production are different:

• In males 4 viable sperm are produced Spermatogenesis

• In females 3 of the cells produce are known as polar bodies and do not survive. Only one egg is formed

Oogenesis

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Differences• The cyctoplasm of the

female oocyte does not divide equally; one of the daughter cells called an ootid, receives most of the cyctoplasm while the other cells called polar bodies (“nurse cells”) die and are reabsorbed to provide nutrients

• Sperms show equal division of cytoplasm; all 4 daughter cells become viable sperm

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• Occurs in the seminiferous tubules where diploid spermatogonia, stem cells that are the precursors of sperm.

•Spermatogonia divide by mitosis to produce more spermatogonia or differentiate into spermatocytes

Spermatogenesis

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• Meiosis of each spermatocyte produces 4 haploid spermatids. This process takes over three weeks to complete

• Then the spermatids differentiate into sperm, losing most of their cytoplasm in the process.

Spermatogenesis

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Sketch Spermatogeneis showing meiotic divisions

1. Spermatogonium

2. 1° Spermatocyte

3. 2° Spermatocyte

4. Spermatid

5. Sperm

46

2323

23 232323

1st Meiotic division

2nd Meiotic division

46

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Oogenesis• Egg formation

takes place in the ovaries.

• the initial steps in egg production occur prior to birth.

• Diploid stem cells called oogonia divide by mitosis to produce more oogonia and primary oocytes

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Sketch Oogeneis showing meiotic divisions

1. Oogonium

2. Oocyte

3. a) 2° Oocyte b) 1st polar body

4. a) Ootidb) polar bodies

5. Ovum

46

2323

1st Meiotic division

2nd Meiotic division

46

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• By the time the fetus is 20 weeks old, the process reaches its peak and all the oocytes that she will ever possess (~4 million of them) have been formed.

• By the time she is born, 1–2 million of these remain. Each has begun the first steps of the first meiotic division (meiosis I) and then stopped.

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• No further development occurs until years later when the female becomes sexually mature.

• Then the primary oocytes recommence their development, usually one at a time and once a month.

Unfertilized oocyte

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• The primary oocyte grows much larger and completes the meiosis I, forming a large secondary oocyte and a small polar body that receives little more than one set of chromosomes. Which chromosomes end up in the egg and which in the polar body is entirely a matter of chance.

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Meiosis: Male and Female Differences

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• In humans, 22 of the 23 are homologous; these are the autosomes

• Thomas Hunt Morgan discovered that having 2 rod shaped (X chromosome) indicated female and 1 rod with 1 hooked shaped chromosome (Y chromosome) identified males

• The X and Y are not homologous, they are the sex chromosomes

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Meiosis and Variation• Unlike mitosis, meiosis does not produce

identical cells

• The cells produced only have half the number but the chromosomes therefore only ½ the genetic information

• What chromosomes end up in what cell all depend upon how the chromosomes line up in Metaphase I

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Meiosis and Variation• If the two blue

chromosomes line up on the same side and the two red chromosomes line up on the same side

• Then the daughter cells will have either the genetic information from the red or blue chromosome

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Meiosis and Variation• If 1 red and 1 blue

line up on the same side

• The daughter cells will have genetic information from both red and blue chromosomes

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MITOSIS MEIOSISPARENT CELL

(before chromosome replication) Site ofcrossing over MEIOSIS I

PROPHASE ITetrad formedby synapsis of homologous chromosomes

PROPHASE

Duplicatedchromosome(two sister chromatids)

METAPHASE

Chromosomereplication

Chromosomereplication

2n = 4

ANAPHASETELOPHASE

Chromosomes align at the metaphase plate

Tetradsalign at themetaphase plate

METAPHASE I

ANAPHASE ITELOPHASE I

Sister chromatidsseparate duringanaphase

Homologouschromosomesseparateduringanaphase I;sisterchromatids remain together

No further chromosomal replication; sister chromatids separate during anaphase II

2n 2n

Daughter cellsof mitosis

Daughter cells of meiosis II

MEIOSIS II

Daughtercells of

meiosis I

Haploidn = 2

n n n n

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Abnormalities during Meiosis

The movement of the chromosomes in a dividing cell is so precise that only 1 in every 100,000 divisions will contain an error

Non-disjunction= an error during meiosis where sister

chromatids fail to come apart resulting in gametes that are missing or have extra chromosomes

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Non-disjunction• One daughter cell

will be missing one of the chromosomes (22)

• Other daughter cell will contain an extra chromosome (24)

• In humans, non-disjunction produces gametes with 22 or 24 chromosomes

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Non-disjunctions• When gamete with 24 chromosomes

joins a normal gamete with 23 chromosomes, the zygote will contain 47 (instead of 46). This zygote will have 3 chromosomes in place of the normal pair = trisomy

• When the gamete with 22 chromosomes joins a normal gamete with 23 chromosomes, the zygote has 45; this zygote will have 1 chromosome in place of the normal pair = monosomy

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• The best way to study non-disjunctions is by looking at karyotypes

• Karyotypes are an inventory of an individuals chromosomes– A karyotype

usually shows 22 pairs of autosomes and one pair of sex chromosomes

KARYOTYPES

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Preparation of a karyotype

Figure 8.19

Blood culture

1

Centrifuge

Packed redAnd white blood cells

Fluid

2

Hypotonic solution

3

Fixative

WhiteBloodcells

Stain

4 5

Centromere

Sisterchromatids

Pair of homologouschromosomes

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Non-disjunctionsA number of disorders are caused by non-

disjunctions1. Down’s Syndrome2. Edward’s Syndrome3. Patau’s Syndrome4. Turner’s Syndrome5. Kleinfelter’s Syndrome6. Other severe abnormalities

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Non-disjunctionsThe risk of

chromosomal abnormalities increases with maternal age because the egg cells are older

Women over the age of 35, who have children increase their chance exponentially

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Karyotype for Down’s SyndromeTrisomy 21

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Down’s SyndromeTrisomy 21Cause: - Non-disjunction of

chromosome #21- Individual has 47

chromosomesKaryotype: - has 3 chromosome #21Symptoms: - mentally & physically

delayed, large forehead, large space between eyes

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What does this karyotype tell us?

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Patau’s Syndrome (trisomy) Cause:

- non-disjunction of chromosome # 13Karyotype: - has 3 chromosome #13Symptoms: - child with multiple and severe abnormalities, and severe mental retardation

-  head very small, eyes absent or very small

- hairlip, cleft palate, usually malformations of internal organs

- most cases child dies soon after birth

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What does this karyotype tell us?

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Edward’s Syndrome: Trisomy 18

Cause: - Non-disjunction of chromosome #18Karyotype: -has 3 of chromosome #18Symptoms: -very small and weak, head flattened, hands short with very little development

- severe mental handicap with life expectancy of less than one year

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What does this Karyotype tell us?

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Klinefelter’s Syndrome (Trisomy 23)Cause: - Non-disjunction sex

chromosomesKaryotype: - 2 X chromosomes and a Y

chromosome (XXY)Symptoms: - Appears male at birth but

upon puberty releases high levels of female hormones

- Sterile males, breast development, slightly feminized physique

- Affects 1/1000 male births

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What does this karyotype tell us?

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Turner Syndrome (Monosomy)

Cause: - Non-disjunction of X chromosome in femalesKaryotype: - females have a single X chromosome (XO)Symptoms: - sterile females, short stature,

underdeveloped gonadal structures- Affects 1/5000 female births

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Non-disjunction in MalesXY XX

XY X X

XXY XO

O

Klinefelter Turner

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Non-disjunction in femalesXY XX

Y XX O

XXY XO

X

Klinefelter Turner

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Other possible abnormalites caused by non-disjunction

-these infants do not live very long – a few days at the most; many are premature and stillborns-These photos may disturb you, you are not required to watch