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45 Terms

1
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What is the process by which bacteria reproduce?

Bacteria reproduce through binary fission.

2
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What type of chromosome do bacteria have?

Bacteria have a circular chromosome.

3
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What initiates replication in bacterial chromosomes?

Replication starts at the origin of the chromosome.

4
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What is the role of the FtsZ protein in bacterial cell division?

FtsZ protein forms a middle septum that allows the cell to divide.

5
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How does the genetic consistency of prokaryotic organisms arise?

Through the clonal reproduction and binary fission process, which ensures each daughter cell gets a complete copy of the chromosome.

6
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What are eukaryotic chromosomes composed of?

Eukaryotic chromosomes are composed of chromatin, which includes 40% DNA and 60% protein.

7
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What is a karyotype?

A karyotype is the particular array of chromosomes in an individual.

8
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What is the diploid number of chromosomes in humans?

Humans are diploid with 46 total chromosomes.

9
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What is chromatin?

Chromatin is a complex of DNA and proteins that make up chromosomes.

10
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What structure allows for the compact packing of DNA in eukaryotic cells?

Nucleosomes facilitate the compact packing of DNA.

11
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What is the primary function of cohesin proteins during cell division?

Cohesin proteins hold sister chromatids together until anaphase.

12
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What are the stages of the eukaryotic cell cycle?

Interphase (G1, S, G2), M phase, and Cytokinesis.

13
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What happens during the G1 phase of the cell cycle?

The cell assesses size, nutrient availability, and DNA integrity.

14
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What occurs during the G2 phase prior to mitosis?

The cell checks for successful DNA replication and DNA damage.

15
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What is the purpose of cytokinesis?

Cytokinesis divides the cytoplasm, resulting in two distinct daughter cells.

16
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What role does the centromere play in mitosis?

The centromere is the point of constriction, serving as the attachment site for the kinetochore.

17
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What distinguishes telophase in the process of mitosis?

Nuclear envelope reforms around the chromatids, and the spindle disassembles.

18
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What is the function of MPF (maturation-promoting factor) in the cell cycle?

MPF induces cell division through phosphorylation.

19
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How do growth factors influence the cell cycle?

Growth factors can override cellular controls that inhibit cell division.

20
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What is the role of p53 in relation to cancer?

p53 is a tumor suppressor gene that monitors DNA integrity and can induce cell death if damage is severe.

21
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What are gametes in sexual reproduction?

Gametes are haploid cells produced through meiosis.

22
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How many rounds of division occur in meiosis?

Meiosis involves two rounds of division, meiosis I and meiosis II.

23
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What is the difference between sister chromatids and homologous chromosomes?

Sister chromatids are identical copies of a single chromosome, while homologous chromosomes are pairs of similar chromosomes from each parent.

24
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What is the significance of synapsis during prophase I of meiosis?

Synapsis is the association of homologous chromosomes, allowing for genetic recombination.

25
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What role does crossing over play in genetic variation?

Crossing over allows for the exchange of genetic material between non-sister chromatids, increasing genetic diversity.

26
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In plant meiosis, how many haploid cells are produced?

Meiosis produces four haploid cells, which may divide mitotically before becoming gametes.

27
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What is the phenotypic ratio expected from a monohybrid cross?

The expected phenotypic ratio is typically 3:1 in the F2 generation.

28
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What defines a dihybrid cross?

A dihybrid cross involves two variations of two traits, exhibiting a phenotypic ratio of 9:3:3:1 in the F2 generation.

29
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What is the principle of independent assortment?

Alleles of different genes assort independently during meiosis.

30
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What is a testcross used for?

A testcross is used to determine the genotype of an individual with an unknown phenotype.

31
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What is pleiotropy?

Pleiotropy refers to a single allele affecting multiple traits or phenotypes.

32
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What is incomplete dominance?

Incomplete dominance is when a heterozygote has a phenotype that is intermediate between the two homozygotes.

33
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What does codominance mean?

Codominance occurs when both alleles of a gene are expressed in the phenotype of the heterozygote.

34
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How do sex-linked traits differ from autosomal traits?

Sex-linked traits are associated with genes found on sex chromosomes and can exhibit different inheritance patterns.

35
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What is dosage compensation?

Dosage compensation is the process ensuring equal expression of genes from sex chromosomes despite different amounts.

36
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How does genomic imprinting affect gene expression?

Genomic imprinting results in the expression of a gene depending on whether it was inherited from the mother or the father.

37
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What is the relationship between recombination frequency and genetic distance?

Recombination frequency is proportional to the genetic distance between loci.

38
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What is the effect of nondisjunction during meiosis?

Nondisjunction can lead to aneuploidy, which is the gain or loss of chromosomes.

39
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What is an example of a recessive genetic disorder?

Cystic fibrosis is an example of a recessive genetic disorder caused by a defect in chloride ion transport.

40
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What type of cells result from meiosis in animals?

In animals, meiosis results in gametes.

41
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What are SNPs (single-nucleotide polymorphisms)?

SNPs are variations at a single base pair in the DNA sequence that can affect genetic traits.

42
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How do mutations in proto-oncogenes contribute to cancer?

Mutations in proto-oncogenes can cause them to become oncogenes, leading to uncontrolled cell growth.

43
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What defines a homozygous genotype?

A homozygous genotype has two identical alleles for a trait.

44
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What does the term 'phenotypic plasticity' refer to?

Phenotypic plasticity is the ability of an organism to change its phenotype in response to environmental conditions.

45
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What is an example of a dominant genetic disorder?

Huntington's disease is an example of a dominant genetic disorder caused by a mutation in the HTT gene.