300816 Lecture 11: Cell biology patterns of inheritance

42 views2 pages

amberhippopotamus661

16 Feb 2019

School

UWS

Department

University of Western Sydney

Course

300816

Professor

anonymous

For unlimited access to Class Notes, a Class+ subscription is required.

Document Summary

Salient points: alleles, phenotype vs genotype, mendel, segregation. Inheritance: genetics can predict how genes may be passed on to future generations, this is affected by: How chromosomes are passed on during meiosis. Alleles: an allele is a specific version of a gene at the same position (locus) on a gene, different alleles code for different forms of the same protein. The different forms of the protein function differently- resulting in different characteristics phenotype vs genotype: diploid organisms have 2 copies of every gene. This means that one individual can have two different versions of a gene. The term allele is used to identify different versions of a gene phenotype: describes the organisms appearance as a result of its genotype genotype, describes the combination of alleles present in the organisms cell, homozygous: 2 copies of the same allele: heterozygous: Heterozygote is intermediate in phenotype between the two homozygous. Heterozygote shows some aspect of the phenotypes of both homozygotes.

Related Questions

These all relate to exceptions to the inheritance patterns encountered by Mendel.â

Why do multiple and lethal alleles often result in modifications of the classic Mendelian monohybrid and dihybrid ratios?

Select the four correct statements.

-When an essential gene is mutated, it can result in a lethal phenotype. There are no classic Mendelian monohybrid and dihybrid ratios.

-In the case of codominance, heterozygotes produce gene products from both alleles of a gene. Classic Mendelian monohybrid and dihybrid ratios are modified by codominance.

-In the case of incomplete dominance, the phenotype of the heterozygote is distinct from and often intermediate to the phenotypes of homozygous individuals. Classic Mendelian monohybrid and dihybrid ratios are modified by incomplete dominance.

-Genes exist in a large number of allelic versions and a diploid organism has two homologous gene loci that may be occupied by different alleles of the same gene. This can result in many different phenotypes for traits, which may not follow typical Mendelian ratios.

-When an essential gene is mutated, it can result in a lethal phenotype. This results in a modification of classic Mendelian ratios.

-The phenotype of the heterozygous genotype is distinct from and often intermediate to the phenotypes of the homozygous genotypes. The joint expression of both alleles in a heterozygote is called codominance. There are no classic Mendelian monohybrid and dihybrid ratios.

-Genes exist in a large number of allelic versions, but in a diploid organism, only one allele of the gene can occupy one homologous gene loci. Classic Mendelian inheritance cannot explain this phenomenon.

-Each gene produces a unique gene product. The effect of one allele in a heterozygote completely masks the effect of the other. Classic Mendelian genetics cannot explain this phenomenon.

Ploidy refers to the number of complete sets of chromosomes (genes) present in a cell. The number of chromosomes in a complete set is a fixed characteristic of a species. Humans are diploid with two sets of 23 chromosomes. Fruit flies are diploid with two sets of 4 chromosomes. Sexually reproducing organisms are diploid, each somatic cell of an organism has two complete sets ("di" is a prefix indicating 2.). To complete a life cycle and reproduce new members of a species, mating is required. Mating brings a donation from a male and a donation from a female together. However, if the male and female cells remain diploid, the fertilization will result in a tetraploid zygote. In general, these are not viable. A mechanism is needed to form special haploid cells, gametes. The diploid set is split precisely into two complete haploid sets. That mechanism is meiosis.

The complete set of chromosomes of a species is also the complete set of genes of a species, the genome. (Yes, there is a minor contribution from mitochondria and chloroplasts. Inheritance of this information is "cytoplasmic".)

Please answer the following questions:

1. How many chromosomes in a brain cell of a fruit fly? How many chromosomes are in a liver cell of a human? Explain both answers.

2. How many chromosomes are in a fruit fly unfertilized egg? How many chromosomes are in a human egg? Explain both answers.

3. Why is meiosis necessary for sexually reproducing organisms? How many chromosomes are in a human zygote? Relate the two answers.

4. What is a gene allele? Suppose there is a gene called "bingo" and it is present once in a complete haploid set. How many alleles of "bingo" does a diploid individual have? How many copies or versions of the gene "bingo" are present in a diploid individual?

5. Modern DNA sequencing clearly identifies alleles by showing the different DNA sequence of each allele. These alleles may be termed structural alleles (I coined the term for this problem.). Classical genetics only dealt with phenotypes or visible traits. As a result, alleles of genes were identified by functionality, usually normal or non-functional. Using your knowledge of gene structure and gene expression, postulate a relationship between structural alleles and functional alleles. (include relative amounts; more, less, or equal).

QUESTION 1

Jim is blood type A, his brother John is type O and his sister Jane is type AB. What are the genotypes of their parents?

Which of the following is true for alleles that show incomplete dominance?

Heterozygotes have a genotype like the dominant allele.

Homozygotes have a genotype like the recessive allele.

Heterozygotes have a phenotype intermediate between the dominant and recessive alleles.