Chapter 4: Chromosome Theory of Inheritance Flashcards

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1
Q

God’s glory in reproduction?

A

God is glorified when His creation reproduces–they are obeying his command, good stewards can be involved

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2
Q

What is the function of chromosomes? What is important?

A

Transmit genetic information
- Important: the type and amount of genetic material for normal development

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3
Q

Types of chromosomes with respect to centromere

A

Metacentric: centromere in middle
Acrocentric: centromere is near one end

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4
Q

Chromosomes with respect to each other (three words)

A

Sister chromatids: identical copies of a replicated chromosome
Homologues: same set of genes, potentially different alleles
Nonhomologues: completely unrelated genes

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5
Q

What is a karyotype?

A

picture/arrangement of chromosomes by length (two of each because diploid)

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6
Q

What determines maleness in humans?

A

SRY gene,
- because of cross over SRY functional in XX males, and SRY nonfunctional in XY females

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7
Q

What is mitosis? What does it produce? What are the phases?

A
  • the cell cycle with repeating patterns of cell growth and division
  • produce: two genetically identical daughter cells
  • mitosis/cytokinesis and interphase
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8
Q

What is interphase?

A

Period of cell growth & chromosome duplications (most of time here)
- formation of microtubule in cytoplasm
– centrosome: microtubule organizing center near the nuclear envelope
– centrioles: core of centrosome, not found in plant cells
Gap 1 phase (G1): cell growth, chromosomes not duplicating or dividing
- G0: stop dividing and arrest
Synthesis phase (S): chromosomes replicate (sister chromatids)
Gap 2 phase (G2): synthesis of proteins for mitosis

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9
Q

What are the stages of mitosis?

A

1) Prophase: chromosomes condense and become visible
2) Prometaphase: spindle forms and sister chromatids attach to microtubules from opposite centrosomes
3) Metaphase: chromosome align at the cell equator
4) Anaphase: sister chromatids separate and move to opposite poles
5) Telophase: chromosomes recondense and are enclosed in two nuclei

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10
Q

What are the two types of cells?

A
  • somatic (most) in G0 or active in mitosis
  • Germ cells (precursors to gametes)
    – set aside during embryogenesis
    – incorporated into reproductive organs
    – meiosis & haploid gametes
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11
Q

What is the overview of meiosis?

A

Two rounds of cell division
- Chromosomes duplicate once; nuclei divide twice
- Meiosis II reduces the chromosomes from 2n to n

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12
Q

What is the overview of meiosis I?

A

Homologs pair, cross over, and then segregate
- sister chromatids remain intact, - maternal/paternal homologs recombine and create new combinations of alleles then segregate to different daughter cells

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13
Q

What are the substages of prophase I?

A

Homologs pair and held together by synaptonemal complex, crossing-over (recombination) occurs
- Leptotene (chromosomes visible, centrosomes opposite poles)
- Zygotene (Homologous chromosomes enter synapsis and synaptonemal complex forms
- Pachytene (synapsis complete, crossing-over occurs)

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14
Q

What occurs after prophase I?

A

Telophase I: nuclear envelope reforms, resulting in half number of chromosomes
Interkinesis: like interphase but no chromosomal duplications

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15
Q

What occurs in meiosis II?

A

sister chromatids separate and move to opposite poles
- Prophase II: chromosomes condense, centrioles moves to opposite poles, nuclear envelope breaks down
- Metaphase II: chromosomes align at metaphase plate, sister chromatids attach to spindle fibers)
- Anaphase II: centromeres divide and sister chromatids move to opposite poles
- Telophase II: chromosomes uncoil & nuclear envelopes & nucleoli reform
- Cytokinesis: cytoplasm divides

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16
Q

What is a mistake in meiosis?

A

Nondisjunction: mistakes in chromosome segregation during meiosis I or II
- nonviable gametes or embryos or abnormal chromosome numbers

17
Q

How does meiosis contribute to genetic diversity?

A

1) Independent assortments of non-homologs creates different combinations of alleles
2) Crossing-over between homologs creates different combinations of alleles within each chromosome

18
Q

What are the pedigree patterns suggesting sex-linked inheritance?

A

X-linked recessive:
- mutation never from father to son
- affected father –> daughters carriers, 1/2 sons inherit trait
X-linked dominant:
- trait in every generation
- affected male –> affected daughters and unaffected sons
Y-linked;
- only in males