Premium Essay

Ptc Taster Genomic Analysis Lab Report

In:

Submitted By hroza
Words 256
Pages 2
Title:

Abstract:

Introduction:
Background:

PTC or phenylthocarbamide is conveyedby a single geneTAS2R38 that codes for a taste receptor on the tongue was eventually identified in 2003.
The ability to taste PTC is usually associated with dominant inheritance where the inability to taste PTC is to be recessive.
For decades, humans were classified as tasters or nontasters.
The goal of this experiment was to determine 1. Taster Phenotype, 2. Isolate DNA from each individual 3. Determine Taster Genotype

Hypothesis:
Ho: If I am a taster, then my genotype for PTC taster must be either TT (homozygous dominant) or Tt (heterozygous)

The traits of being able to taste versus the inability to taste follows the mendelian inheritance. In mendelian inheritance when two heterozygous dominant parents were mated, genotypic ratios were…..

Methods:
This experiment aimed to investigate the allele frequency of the PTC taster gene (TAS2R38) in a small population, represented by the students in class.
To determine the genotypic profile of the students PTC gene,a sample of DNA was extracted using Chelex resin. Polymerase chain reaction was then used to amplify then digest the gene of TAS2R38 gene with a restriction enzyme. Digested DNA will be cut into 2 fragments 239 bp and 64 bp in length. (Figure 2)
This discrepancy in length allowed us to profile the alleles using gel electrophoresis: non-tasters have only the uncut fragment, taster homozygotes the...The enzyme could either cut the enzyme or leave it whole producing a restriction fragment polymorphism that can be separated by agarose gel

Similar Documents

Premium Essay

Ptc Taster Genomic Analysis Lab Report

...PTC Taster Genomic Analysis Lab Report Laboratory Goals: 1. Determine Taster Phenotype 2. Isolate DNA from each individual 3. Determine Taster Genotype Hypothesis: If I am a taster, then my genotype for PTC taster must be either TT (homozygous dominant) or Tt (heterozygous) I – Results: This experiment aimed to investigate the allele frequency of the PTC taster gene (TAS2R38) in a small population, represented by the students in class. The genotype obtained from genomic analysis (via PCR and gel electrophoresis) confirmed that the genotypic result is consistent with the phenotypic result observed at the beginning of the lab. However, DNA fragments of 3 lab subjects didn’t show up on the gel. The allele frequencies can’t be calculated because the data is insufficient to apply the Hardy-Weinberg equation. There are many factors that might be contributed to the invisibility of these DNA fragments, most likely accidental errors. For example, the DNA wasn’t loaded onto the gel probably, or the DNA for some reason didn’t sink to the bottom of the well, or just simply there was not enough DNA. To determine the genotypic profile of the students PTC gene, DNA samplers from each individual was collected from saliva. Using premade PTC primers (short oligonucleotides), a DNA template that encoded the PTC gene (approximately, 303 bp) was amplified by PCR. After amplification, the produced DNA fragments were digested with Fnu4H1 to identify if the lab subjects...

Words: 1197 - Pages: 5