chapter 12 study guide Flashcards

1
Q

How did Gregor Mendel perform cross-pollination in his experiments with pea plants?

A

Mendel removed the male parts from one plant and added pollen from another plant to cross-pollinate.

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2
Q

Who is considered the father of genetics, and what organism did he use for his experiments

A

Gregor Mendel is the father of genetics. He used pea plants for his experiments.

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3
Q

What is a gene, and how is it passed from one generation to the next?

A

A gene is a part of DNA that determines traits. It is passed down from parents to offspring.

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4
Q

What is the difference between homozygous dominant and homozygous recessive?

A

Homozygous dominant has two dominant alleles (like AA), and homozygous recessive has two recessive alleles (like aa).

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5
Q

Define heterozygous and give an example.

A

Heterozygous means having two different alleles (like Aa).

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6
Q

What is incomplete dominance? Provide an example of a trait that exhibits incomplete dominance

A

Incomplete dominance is when neither allele is fully dominant, creating a mix of traits. Example: red + white flowers = pink flowers.

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7
Q

Explain codominance and give an example of a trait that shows codominance.

A

Codominance happens when both alleles are fully expressed. Example: cattle with both red and white patches.

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8
Q

What is polygenic inheritance, and what are some examples of traits controlled by multiple genes?

A

Polygenic inheritance is when many genes control a trait. Examples: skin color and height.

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9
Q

What is mitosis, and why is it important?

A

Mitosis is when a cell divides to make two identical cells. It’s important for growth and repair.

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10
Q

What happens during crossing over in meiosis, and why is it important for genetic diversity?

A

Crossing over is when chromosomes exchange DNA, making genetic diversity by mixing genes.

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11
Q

What occurs in Metaphase II of meiosis, and how does it resemble Metaphase of mitosis?

A

In Metaphase II, chromosomes line up in the middle of the cell, just like in mitosis.

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12
Q

What are chromosomes, and how do they carry genetic information?

A

Chromosomes are structures made of DNA that carry genes, which determine traits.

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13
Q

How many chromosomes do humans have, and how are they inherited?

A

Humans have 46 chromosomes (23 pairs). One set comes from each parent.

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14
Q

What are homologous chromosomes, and why are they important in inheritance?

A

Homologous chromosomes are pairs of chromosomes with similar genes, one from each parent. They are important because they carry the same genes but can have different versions of alleles.

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15
Q

What is the difference between diploid and haploid cells?

A

Diploid cells have two sets of chromosomes (2n), while haploid cells have one set (n). Diploid cells are body cells, and haploid cells are sperm and egg cells.

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16
Q

Explain the concept of nondisjunction and describe its potential consequences for an organism.

A

Nondisjunction is when chromosomes don’t separate correctly during cell division. This can cause too many or too few chromosomes, leading to genetic disorders.

17
Q

How does nondisjunction lead to genetic disorders like Down syndrome?

A

Nondisjunction can cause an extra chromosome 21 in a gamete. If this gamete combines with another, the child will have three copies of chromosome 21, leading to Down syndrome.

18
Q

what’s the difference between mitosis and meiosis.

A

mitosis: body cells, 1 division, no cross over, genetically identical cells, 2 diploid.

meiosis: gametes, 4 haploid, 2 division, crossing over, genetically different cells.