BIOL 2905 Lecture Notes - Lecture 21: Zygosity, Mitosis, Aneuploidy

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lavendershark790

25 Oct 2017

School

York University

Department

Biology

Course

BIOL 2905

Professor

Dasantila Golemi- Kotra

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Document Summary

Independent assortment & random segregation: one chromosomes in not influencing the segregation of another, completely random & independent of one another, how many possible combinations, 2n organisms 2n. Independent assortment in meiosis: individual heterozygous at 2 genes (loci)- genes are on different chromosomes, locus describes location of gene on chromosome, meiosis results in 4 haploid cells that. Combinations of gametes in fertilization: allows for more variability- which sperm cell & which egg cells combines, each egg & sperm cell has different genes. Comparison of meiosis & mitosis: mitosis in anaphase, the sister chromatids are spilit; same with meiosis, mitosis is 2 identical daughter cells; meosis produces 4 different cells. Mistakes in meiosis: non-junction: failure of chromosomes segregation in meiosis i or meiosis ii, when separation during anaphase is not equal, it can occur in meiosis one or meiosis 2. Results in offsprings with incorrect number of chromosomes: euploids: normal number of chromosomes, aneuploid: extra or missing chromosomes.

Related Questions

Which statements pertaining to genetic variability are correct? Check all that apply (note that wrong answers will be deducted from right answers)!

Crossing over is defined by the exchange of chromosome pieces during metaphase one of meiosis.

If a germ cell (i.e. parent cell before meiosis) had only two pairs of homologous chromosomes (i.e. 4 chromosomes total) there are 2 possible combinations of maternal and paternal chromosomes in gametes.

Siblings produced by sexual reproduction are different because sperms are different from one another and eggs are different from one another, and the combination of an egg and sperm is basically unique.

Random fertilization means that all possible combinations of eggs and sperm are equally likely, i.e. it is pure chance which sperm fuses with which egg.

Individual chromosomes contain thousands of genes. This means that during each crossing over event, more than one gene is exchanged between paternal and maternal chromosomes.

limedonkey586

1. What is the chromosome theory of inheritance?

2. Understand how independent assortment can cause gametes to have four combinations of alleles when an individual is heterozygous for two genes on two different chromosomes.

3. What are linked characters and linked genes? Understand why linked genes will not independently assort.

4. How can crossing over affect linked genes?

5. What are recombinant gametes?

6. Define recombinant frequency. Be able to use the recombinant frequency to determine how close two genes are on a chromosome.

7. What is a linkage map?

8. What is the function of the SRY gene on the Y chromosome? What happens if you don't have this gene?

9. Know how sex is determined in mammals, birds, bees and ants, and reptiles.

10. How many autosomes and sex chromosomes do normal human haploid and diploid cells have?

11. What does it mean for a gene to be X-linked or Y-linked?

12. Be able to answer word problems and fill out a Punnet square involving an X-linked recessive trait.

13. Which sex is more likely to have an X-linked recessive disorder? Understand why.

P.s The most simple answer would be preferable. I would be copping the notes over that you will provide to my noteb book and add my details to it.

greylocust179

Which of these statements is incorrect?

Syntenic genes are located on the same chromosome.

Independent assortment results in recombinant chromosomes.

You can reliably predict the relative genetic distance fromgenesâ physical distance on a chromosome.

Linked genes are always syntenic.

What is the relative genetic distance between two linked genesif the recombination frequency is 0.49?

0.49 cM

4.9 cM

49 cM

490 cM

What statement best explains the distortion in Mendelian ratiosobserved by Bateson & Punnett in 1905? (Reminder: they found anoverrepresentation of F2 offspring showing both dominant orrecessive phenotypes, and an underrepresentation of offspringdisplaying one dominant and one recessive phenotype)

Human error: they should have been more careful about theirexperimental setup.

Gene linkage: Genes for flower color and pollen shape arephysically close on the same chromosome, leading to a breakdown inthe independent assortment of the alleles for these traits.

Chromosome crossover: Homologous recombination of twochromatids during meiosis caused the alleles to shuffle, resultingin a breakdown of the independent assortment of the alleles forthose genes.

Random variation: No two situations are alike. In finitepopulations, you are going to get some variation across a mean.

When determining the relative genetic distance between twogenes, why is dihybrid back-cross preferable over traditionaldihybrid cross?

9:3:3:1 phenotypic ratio is easier to work with than 1:1:1:1ratio.

Genotypes of the offspring can be determined based on theirphenotype.

If the genes are independently assorted, the dihybrid back-crosswould result in only 2 genotypes in the F1 generation.

B and C

Why do we map genes?

To understand how genes interact with each other

Comparative genomics analysis