Topic 3- Genetics Flashcards

1
Q

What is DNA?

A

DNA is a chemical that carries genetic information and is found in the chromosomes, which are found in the nucleus of most cells.

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2
Q

What does DNA stand for?

A

Deoxyribose Nucleic Acid.

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3
Q

What are the 4 complementary base pairs?:

A

The complementary base pairs join the strands in a double helix of DNA together they are

  • adenine
  • thymine
  • cytosine
  • guanine
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4
Q

What base pairs in DNA go together and why?

A

A-T go together and C-G go together.
This is because between the base pairs there are hydrogen bonds.
Parts of the DNA bases are slightly charged. A slightly negative charged base attracts a slightly positive charged base. THIS FORMS A WEAK HYDROGEN BOND.

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5
Q

What is the shape of DNA?

A

A molecule of DNA contains 2 strands that form a helix. The two strands are joined together by the complementary base pairs to form a double helix.

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6
Q

What is a genome?

A

The genome is the entire length of your DNA.
(The nuclei of your cells contain very long molecules of dna each molecule is tightly folded and cooled to make a chromosome.)

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7
Q

What is the DNA code?

A

The order of bases in a gene contain the coded instructions for a protein. We have different genes because of the slight differences I the order of our bases.

Everyone has different DNA except identical twins.

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8
Q

What does RNA stand for?

A

Ribonuclease acid

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9
Q

In protein synthesis what are the bases and what are the bases

A
  • adenine
  • cytosine
  • guanine
  • uracil

U replaces T so the base pairs are:
C-G
A-U

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10
Q

Explain the basic steps of transcription in protein synthesis?

A

1) an enzyme called RNA polymerase attaches to the DNA.
2) It attaches to the DNA in front of a non coding region (called non coding region because it contain ps no code for a protein)
3) The enzyme separates the 2 DNA strands .
4) The enzyme moves along the DNA strand (the template strand) adding complementary nucleotides.
5) The nucleotides link to form a strand of messenger RNA (mRNA).

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11
Q

Describe the basic steps of translation in protein synthesis?

A

1) The mRNA strand travel out the nucleus through nucleur pores.
2) In the cytoplasm The mRNA strands attach to ribosomes.
3) a ribosome moves along a mRNA stand 3 bases at a time. EACH TRIPLET OF BASES IS CALLED A CODON.
4) At each mRNA codon a molecule of transfer RNA (tRNA) with bases line up.
5) Each tRNA molecule carries a specific amino acid.
6) As the ribosome moves along it joins the amino acids from tRNA molecules together to form a polypeptide chain.

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12
Q

What are Mendel’s 3 laws of inheritance?

A
  • Each gamete receives only one factor for characteristics.
  • The version of a factor that a gamete receives is random and does not depend on the other factors in a gamete.
  • Some versions of a factor are more powerful than others and always have an effect of the offspring.
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13
Q

What is an allele?

A

Different forms of the same genes are called alleles

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14
Q

What does homozygous mean?

A

If both alleles for 1 gene are the same an organism is homozygous for that gene. This is the more dominant.

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15
Q

What does heterozygous mean?

A

If alleles are different for one gene. This is the less dominant genotype.

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16
Q

Describe what phenotype and genotypes are?

A

Genotype: The allele of an organism.(Its gene)

Phenotype: What an organism looks like.

17
Q

When are recessive characteristics seen?

A

A recessive characteristic is only seen if both alleles are recessive.

18
Q

In punnet squares what letters represent male female ?

A

The egg cell contains X chromosomes and the sperm contains X&Y chromosomes.

IT IS THE SPERM CELL THAT DETERMINES THE SEX OF THE OFFSPRING.

19
Q

What is the ABO blood group?

A

Everyone’s blood is one of four blood groups. A, B, AB, O. Which blood group you have is determined by weather you have a certain ‘marker molecule’ on the outside of your red blood cells.

The marker molecules are A, B, O.

20
Q

What does co-dominant mean and give an example?

A

Co-dominance occurs when both the alleles for a gene affect the phenotype.
A B
A person with a (blood) genotype I and I Shoe the affects of both blood groups AB.

21
Q

What is melanin?

A

The OCA2 gene controls the amount of melanin produced. Melanin is a protein that controls the colour of hair skin and eye colour and the darkness of it.

The more melanin someone has the darker their hair skin and eye colour.

22
Q

When do mutations occur?

A

Mutations can be caused by:

  • a change in the bases of genes
  • When DNA is not copied properly in cell division
  • environmental factors.

THIS IS MORE LIKELY TO HAPPEN IF THERE IS DAMAGE TO THE DNA BY RADIATION CERTAIN SUBSTANCES.

23
Q

What are the 3 possible phenotypic outcomes from a genetic mutation?

A
  • A genetic mutation results in no change to the phenotype.
  • a genetic mutation could result in a small change to the phenotype.
  • a genetic mutation can rarely, lead to a large change in the phenotype.
24
Q

How is genetic variation caused?

A

This is caused by different alleles inherited during sexual reproduction.

25
Q

What are polypeptides and how are they made?

A

As the ribosomes move along the DNA it joins the amino acids from the tRNA molecules together forming a polypeptide.

A POLYPEPTIDE IS A CHAIN OF AMINO ACIDS.

26
Q

Sex linkage disorders:

A

Chromosomes in diploid cell comes in pairs. Most chromosomes have the same genes however the male human Y sex chromosome is shorter that the X and therefore is missing some of the genes found on X. This means a man may only have one allele for some genes of the X chromosome and if there is a genetic disorder he will inherit it.