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Laabri

4.6 Karyotype Lesson

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Last updated about 2 hours ago
18 Nsɛmmisa
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Question 1
01:10
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Asemmisa {{asɛmmisaAhyɛnsode}}
1.

How many pairs of chromosomes do humans have?

Question 2
02:21
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Asemmisa {{asɛmmisaAhyɛnsode}}
3.

A centriole is a small, cylindrical organelle made up of microtubules, found in animal cells and some lower plant cells. Centrioles play a key role in cell division by helping to organize the mitotic spindle, which separates chromosomes during mitosis and meiosis. The cytoplasm is the jelly-like substance that fills the inside of a cell, excluding the nucleus. It is made up of cytosol (the fluid portion), organelles, and various molecules necessary for cellular processes.

The centromere is the region of a chromosome where the two sister chromatids are held together. It plays a crucial role in cell division by serving as the attachment site for spindle fibers during mitosis and meiosis, ensuring proper chromosome separation. The centromere can be located in different positions on a chromosome, influencing its shape.

What is the middle of this chromosome called?

Asemmisa {{asɛmmisaAhyɛnsode}}
4.

The two chromosomes together are considered ___________________ because one is from Mom and one is from Dad.

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5.

How many total chromosomes in this Karyotype? (count the centromeres)

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8.

How many total chromosomes in this cell?

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11.

Which chromosome number has the mutation?

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12.

Which chromosome number has the mutation?

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13.

Nondisjunction is the failure of chromosomes to separate properly during cell division.

A normal cell is supposed to have "n", which is 2 chromosome(s)

But if nondisjunction occurs, then the cell could be "n-1", meaning it has chromosome(s) or the cell could be "n+1", meaning it has chromosome(s)

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14.

Nondisjunction is the failure of chromosomes to separate properly during cell division. What is a possible consequence of nondisjunction in gametes?

Asemmisa {{asɛmmisaAhyɛnsode}}
15.

Structural Chromosomal Mutations

  1. – A part of a chromosome is missing or removed, leading to the loss of genetic material.

  2. – A segment of a chromosome is copied and appears more than once, resulting in extra genetic material.

  3. – A chromosome segment is reversed end-to-end, altering the gene sequence but not the amount of genetic material.

  4. – A piece of one chromosome breaks off and attaches to a non-homologous chromosome, leading to a rearrangement of genetic material.

Mmuae Afoforo a Wobɛpaw:
inversion
deletion
translocation
duplication
Asemmisa {{asɛmmisaAhyɛnsode}}
16.
Draggable itemarrow_right_altCorresponding Item

translocation

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duplication

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deletion

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inversion

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17.

Which type of mutation is shown in the diagram?

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18.

Which type of mutation is shown in the diagram?

Asemmisa {{asɛmmisaAhyɛnsode}}
2.

Turner's is an extra Y chromosome for boys.

Asemmisa {{asɛmmisaAhyɛnsode}}
6.

Is this cell diploid (double chromosomes) or haploid (half chromosomes)?

Asemmisa {{asɛmmisaAhyɛnsode}}
7.

Is this person a male or female?

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9.

Is this cell diploid (2n) or haploid (n)?

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10.

Is this karyotype for a male or female?