QuBi/bio203

BIOL 203 Lab 4. Bioinformatics Exercises

Research in modern molecular genetics increasingly rely on genomic information and computation. The following exercises will expose you to the field of bioinformatics, including the use of online databases and statistical analysis of genetic data.

Introduction

DNA and its organization into genes makes up an organism's genotype. The expression and presentation of those genes in the organism's development, physiology, and physical appearance (physical traits) make up the phenotype of the organism. Phenotypic variations among individuals of a species (e.g., humans) are caused by genotype variations, environmental factors, and interactions between genetic and environmental factors. In other words, phenotypic variations among individuals often have complex, unclear mechanisms and are not necessarily due entirely to genetic differences.

In this lab section, we will explore the concepts of phenotype and genotype by looking at the variations in the TAS2R38 gene, which is responsible for part of the sensation of taste. The taste receptor protein TAS2R38 (taste receptor 2, member 38) has been associated with the ability to taste the bitter compound phenylthiocarbamide (PTC) (Kim et al. 2003). Although most people can taste PTC ("tasters"), a centain percentage of people cannot ("nontasters"). In this experiment, you will test your Taster phenotype as well as determine your Taster genotype and correlate the phenotype with the genotype data. Your results and those of your classmates will be combined to statistically validate if there is such a phenotype-genotype association.

Learning goals and outcomes

Understand phenotype, genotype, and their association
Be able to use the NCBI online databases
Be able to predict genotype frequencies using Hardy-Weinberg equilibrium
Be able to use the contingency test of genotype-phenotype associations

Computer Exercise 1. Search for gene information using NCBI online databases

Point your browser to the NCBI Human Genome Resource page
Type in the "Find A Gene" search box "TAS2R38" and select "Homo sapiens" from the pull-down menu. Click "Go"
Select the first link, which leads to an NCBI Gene Card page. Use the Gene Card to identify the following information on TAS2R38 gene:
1. NCBI GeneID
2. Chromosome location
3. Click on "GenBank" and identify its gene structure, including the length of primary transcript, coding sequences, 5'-UTR and 3'-UTR. Does it have any introns?
4. Zoom out the Sequence View to find its neighboring genes. Zoom out to read DNA sequences.
Click the link to OMIM (under Phenotype) and find phenotypes associated with TAS2R38 gene
1. What does OMIM stand for?
2. What are the expected "taster" and "nontaster" frequencies within human populations?
3. If the ability to taste bitterness is evolutionary advantageous, how are alleles contributing to "nontaster" maintained in population?
4. Is the correlation between TAS2R38 gene variations and the PTC phenotype variations 100%? If not, what could be the other causes?

Computer Exercise 2. Predict results of PCR and restriction analysis

On a printout of the DNA sequence of TAS2R38 gene (from the GenBank link, see above),

Identify 5'-UTR, 3'-UTR, start codon, and stop codon.
Identify the regions your PCR primers should bind using the Primer3 web server
1. Point your browser to Primer3 Web Server
2. Select "check_primer" in the top box, and "HUMAN" in the 2nd box
3. Paste the raw gene sequence into the 3rd box: Go to the GenBank page and click "FASTA" near the top of page
4. Paste the two primer sequences into the 4th and 6th boxes
5. Click "Pick Primers"
Identify the base location that contains 785 C/T SNP
Copy and paste the expected 302-bp section and locate the Fnu4H1 site using the NEBcutter website
What are the expected lengths for the C/C, C/T, and T/T genotypes?

Statistics Exercise 1. Test Hardy-Weinberg Equilibrium

The Hardy-Weinberg Equilibrium (HWE) predicts the genotype frequencies at a genetic locus in a random-mating population. If two alleles (e.g., C, T) are segregating in a diploid population with respective frequencies of p and q, if the mating is random, and if there is no fitness difference between the two alleles, then the genotypes frequencies (expected from random Mendelian segregation) are stably maintained throughout the generations with the following values: C/T (2pq), T/T (q²), and C/C (p²).

1. After PCR/sequencing experiments, collect genotype frequencies in your class as a group using the following table:

Table 1. Observed Genotype Frequencies

	C/C	C/T	T/T	Total
Count	N_CC	N_CT	N_TT	N
Frequency	f_CC	f_CT	f_TT	1

2. Calculate SNP allele frequencies using the following formula:

f_C=(2N_CC + N_CT)/N
f_T=(2N_TT + N_CT)/N

3. Predict expected genotype frequencies using HWE:

Table 2. Predicted Genotype Frequencies

	C/C	C/T	T/T	Total
Frequency	f_C x f_C	2 x f_C x f_T	f_T x f_T	1
Count	(multiply the above by N)	(multiply the above by N)	(multiply the above by N)	N

4. Test the goodness-of-fit between the observed (Table 1) and expected (Table 2) genotype frequencies using the Chi-Squared Test:

Χ² = ∑[(N_observed - N_expected)²/N_expected]

5. Exit Questions

1. Compare your Χ² value with the critical value of Χ² (with 2 degrees of freedom)=5.99. If your value is greater than 5.99, it is considered statistically significant at the level of p=0.05. It means that there is less than a 1 to 20 chance of getting a value equal or greater than your value. A significant Chi-squared value in this case would suggest a deviation from HWE.
2. What are the possible causes of deviation from HWE? Biological? Statistical?
3. However, if your result is not significant, the interpretations could be either (1) in support of HWE, or (more scientifically) (2) there is no evidence for deviation from HWE.

Statistics Exercise 2. Test phenotype-genotype assoication

After your PCR/sequencing, collect genotype frequencies in your class as a group
Collect both the genotype and phenotype information using the following table
Test the goodness-of-fit of observed frequencies with expectations from no-association (Null Hypothesis) by using Fisher's Exact test
Exit Questions
1. What is your p value? Is it statistically significant?
2. What are the possible causes of deviation from HWE? Biological? Statistical?