Bio H | Unit 6: Meiosis and Chromosomes

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Last updated 3:46 PM on 5/14/26
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58 Terms

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somatic cells

all cells in the body BUT sperm and egg

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homologous chromosomes

2 chromosomes (one from mom and one from dad) that carry the same genes, same size, and same pattern

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diploid or 2n

have both sets of homologous chromosomes

humans: 2n=46

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gametes

sperm and egg cells, contain one of each chromosome

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haploid or n

have one set of chromosomes, n=23

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how many chromosomes does a chicken have?

78

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how many chromosomes does a fruit fly have?

8

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how many chromosomes does rice have?

24

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meiosis

 Def: Special process to make gametes with half the number of chromosomes (haploid number=n)

•Or reduction division

•Separate homologous chromosomes so only one of each chromosome is in each gamete

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what does meiosis 1 do?

Homologous chromosomes split into 2 different cells (PMAT1)

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what does meiosis 2 do?

Chromatids of each chromosome split into 4 different cells (PMAT2)

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<p>describe prophase 1</p>

describe prophase 1

•Homologous chromosomes pair up

•Also called synapsis

•Form a tetrad = 4 chromatids

•While in this stage, pieces of chromatids can break off and exchange

•Called crossing over

•Make new gene combinations

•Can be called recombinations or recombinants

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what is synapsis

when homologous chromosomes pair up

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<p>what is crossing over</p>

what is crossing over

when pieces of chromatids break off and exchange

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metaphase 1

Tetrads line up at equator

Line up independently

Called independent assortment

Creates unique cells

Increases genetic diversity

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<p>what is independent assortment</p>

what is independent assortment

genes for different traits segregate independently during gamete (sperm/egg) formation

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Anaphase 1 + Telophase 1

Homologous chromosomes move to opposite ends and the cell splits

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<p>Cytokenesis</p>

Cytokenesis

• 2 haploid cells are formed

• Each has one of each homologous chromosome

• Identical Cells

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Prophase 2

there is no DNA replication between the two divisions, no S, no tetrads

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metaphase 2

chromosomes line up single file

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anaphase 2

each chromosome splits into 2 chromatids, become chromosomes as they separate

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telophase 2

2 cells divides into 4 cells, each is haploid and unique

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meiosis 1

knowt flashcard image
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meiosis 2

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spermatogenesis

In males, 4 unique cells made by meiosis become sperm, begins after puberty

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oogenesis

In females, 1 of the 4 cells becomes an egg, the other 3 are not involved in reproduction, begins after birth, process continues after puberty

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autosomes

Human chromosomes #1-22

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sex chromosomes

• Human chromosome pair #23

• Can be XX or XY (not necessarily homologous)

• X and Y carry different genes

• Inherited differently if on X chromosome (men only have 1 copy)

• SRY gene found on Y chromosome- cause start of male 

development

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XX chromosomes?

female

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XY chromosomes?

male

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what system do grasshoppers use to identify gender?

XO

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what system do chickens use to identify gender?

ZX

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what system to bees use to identify gender?

haploid-diploid

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nondisjunction

Chromosomes do not separate correctly in Meiosis

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what does nondisjunction look like in meiosis 1?

•Homologous chromosomes don’t separate correctly

•All 4 haploid cells have incorrect number: n+1, n+1, n-1, n-1

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what does nondisjunction look like in meiosis 2?

•Sister chromatids don’t separate correctly

•2 cells abnormal, 2 normal: n+1, n-1, n, n

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aneuploidy

One or more missing or extra chromosomes

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trisomy

3 of one chromosome

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monosomic

1 of one chromosome

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trisomy 21

down syndrome

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trisomy 18

edwards syndrome

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trisomy 13

patau syndrome

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what is klinefelter syndrome?

-XXY

-Males born with Klinefelter syndrome may have low testosterone and reduced muscle mass, facial hair, and body hair. Most males with this condition produce little or no sperm.

•Treatment may include testosterone replacement and fertility treatment

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<p>what is turner syndrome? (thats not obsessing over alex turner)</p>

what is turner syndrome? (thats not obsessing over alex turner)

•Symptoms include short stature, delayed puberty, infertility, heart defects, and certain learning disabilities.

•Treatment involves hormone therapy. Fertility treatment may be necessary for women who want to become pregnant.

<p><span style="background-color: transparent; font-family: &quot;Times New Roman&quot;, serif;"><span>•Symptoms include short stature, delayed puberty, infertility, heart defects,&nbsp;and certain learning disabilities.</span></span></p><p><span style="background-color: transparent; font-family: &quot;Times New Roman&quot;, serif;"><span>•Treatment involves hormone therapy. Fertility treatment may be&nbsp;necessary for women who want to become pregnant.</span></span></p>
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polyploidy

-More than 2 complete sets of chromosomes

•Triploidy or Tetraploidy

•Plants

•Animals

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what are the 4 variations of chromosome structure?

deletion, duplication, inversion, reciprocal translocation

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<p>deletion</p>

deletion

part of the chromosome (# of genes) is removed

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<p>duplication</p>

duplication

a section of the chromosome is doubled

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<p>inversion</p>

inversion

gene order flipped around

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<p>reciprocal translocation</p>

reciprocal translocation

non-homologous chromosomes, for example: removed from chromosome #13 then moved to chrom. #16

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Describe how different events during meiosis contribute to genetic diversity. Include specific details and terms that apply. Be sure to discuss when these events occur

  1. crossing over - pieces of chromatids and sections of DNA break off and exchange with other chromatids, mixing genes up → more diverse (PROPHASE 1)

  2. independent assortment - genes for different traits segregate independently during gamete (sperm/egg) formation (METAPHASE 1) (different arrangements of x’s - shaded/shaded)

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<p><span><span>Sketch examples of crossing over and independent assortment.</span></span></p>

Sketch examples of crossing over and independent assortment.

knowt flashcard image
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Describe the difference between autosomes and sex chromosomes.

autosomes - chromosomes #1-22

sex chromosomes - chromosome #23 (X AND Y, carry different genes, SRY gene on Y chromosome - start of male development)

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Give 3 examples of how different animals use sex chromosomes to determine chromosomal basis of gender.

humans use XY system

  • grasshoppers use XO system, M: X, F: O

  • chickens use ZW system, M: Z, F: W

  • bees use haplo-diploid, M: 16 all are haploid, F: 32 all are diploid

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Sketch examples of alteration of chromosomal structure (look on lab too)

knowt flashcard image
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Describe ONE example of a human disorder caused by either changes to chromosome number or structure. Give the # of chromosome involved and the characteristics/symptoms/effects of the disorder. 

Trisomy 21 - Down Syndrome

  • an individual has 47 chromosomes, not 46

  • has 3 copies of chromosome 21 instead of the normal 2

  • symptoms/side effects: intellectual disability, developmental delays, and distinct physical traits like a flat facial profile, small ears/mouth, almond-shaped eyes, or poor muscle tone

<p>Trisomy 21 - Down Syndrome</p><ul><li><p>an individual has 47 chromosomes, not 46</p></li><li><p>has 3 copies of chromosome 21 instead of the normal 2</p></li><li><p><span><span>symptoms/side effects: intellectual disability, developmental delays, and distinct physical traits like a flat facial profile, small ears/mouth, almond-shaped eyes, or poor muscle tone</span></span></p></li></ul><p></p>
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Summarize the experiments and conclusions from the reading activity: Naked Mole Rats are Fertile until they Die

from paper:

  • in summary of the article, scientists have discovered that maked mole rats can breed for their entire life, not get cancer, not feel pain, and live for around 37 years.

notes:

  • reproduce for their entire life

  • live in colonies with a queen

  • dont get cancer

  • live for 37 years

  • they keep producing new eggs after they are born