Difference between revisions of "MSymond1 Week 2"

From LMU BioDB 2024
Jump to navigation Jump to search
(figure 6)
(added purpose)
Line 1: Line 1:
−
===Methods and Results===
+
===Purpose===
 +
The purpose of this lab is to study what has been found in the genetics and biochemistry sections of the lab, but diving deeper into the molecular biology of the different colors, and to determine what differences in the DNA sequences lead to the differences in phenotypes seen when the flowers are crossed either with themselves or with others.
 +
====Methods and Results====
 
The software Aipotu was used for this lab, using the molecular biology tab. The completion of the molecular biology section of this lab did require assistance from the group that completed the genetics portion and the biochemistry portion. They helped provide a list of all different alleles, as well as which alleles are true breeding. The molecular biology tab of this software displays the entire DNA and protein sequence of the alleles and what color pigment they make. The first DNA sequence edited in this experiment was the sequence from the red flower. The base that was edited was from the red sequence, and the base was base #20. It was changed from a G to a C. This led the protein sequence to not be folded, because it did not allow for methionine to be coded, therefore, no pigmented protein could be created, making it a white flower. This led to the discovery that there are multiple ways to create a white flower, because any DNA sequence that does not create a functional pigmented protein will create a white flower (figure 1). Using the knowledge of the different alleles, provided by the genetics group, as well as the biochemistry of a purple allele from the biochemistry group, a purple allele for flowers was created using the molecular biology of the organisms to create a true breeding purple organism (figure 2). The three aromatic amino acids that are responsible for color are phenylalanine, tyrosine, and tryptophan. The red sequence from a purple heterozygote had phenylalanine, and the blue sequence had tyrosine. So an amino acid sequence was created that had both of those amino acids. This was done by changing base 82 of a blue sequence to a U, giving it a phenylalanine.  
 
The software Aipotu was used for this lab, using the molecular biology tab. The completion of the molecular biology section of this lab did require assistance from the group that completed the genetics portion and the biochemistry portion. They helped provide a list of all different alleles, as well as which alleles are true breeding. The molecular biology tab of this software displays the entire DNA and protein sequence of the alleles and what color pigment they make. The first DNA sequence edited in this experiment was the sequence from the red flower. The base that was edited was from the red sequence, and the base was base #20. It was changed from a G to a C. This led the protein sequence to not be folded, because it did not allow for methionine to be coded, therefore, no pigmented protein could be created, making it a white flower. This led to the discovery that there are multiple ways to create a white flower, because any DNA sequence that does not create a functional pigmented protein will create a white flower (figure 1). Using the knowledge of the different alleles, provided by the genetics group, as well as the biochemistry of a purple allele from the biochemistry group, a purple allele for flowers was created using the molecular biology of the organisms to create a true breeding purple organism (figure 2). The three aromatic amino acids that are responsible for color are phenylalanine, tyrosine, and tryptophan. The red sequence from a purple heterozygote had phenylalanine, and the blue sequence had tyrosine. So an amino acid sequence was created that had both of those amino acids. This was done by changing base 82 of a blue sequence to a U, giving it a phenylalanine.  
 
[[File:modifiedred.png|200px|thumb|right|Figure 1]]
 
[[File:modifiedred.png|200px|thumb|right|Figure 1]]
 
[[File:purpleorganism.png|200px|thumb|right|Figure 2]]
 
[[File:purpleorganism.png|200px|thumb|right|Figure 2]]
−
====Specific Tasks====
+
=====Specific Tasks=====
 
A) There are no differences in the Green DNA sequences in the Green-1 flower. The differences between blue and yellow sequences in Green-2 were at positions 79, and 80. The differences between the red and white sequences in the red flower are at position 7. There were no differences between the white sequences in the white flower. Between every available allele of the colored (non-white) flowers, all of the differences in the DNA sequences fell in bases 79 and 80
 
A) There are no differences in the Green DNA sequences in the Green-1 flower. The differences between blue and yellow sequences in Green-2 were at positions 79, and 80. The differences between the red and white sequences in the red flower are at position 7. There were no differences between the white sequences in the white flower. Between every available allele of the colored (non-white) flowers, all of the differences in the DNA sequences fell in bases 79 and 80
 
*See figure 3
 
*See figure 3

Revision as of 22:05, 24 January 2024

Purpose

The purpose of this lab is to study what has been found in the genetics and biochemistry sections of the lab, but diving deeper into the molecular biology of the different colors, and to determine what differences in the DNA sequences lead to the differences in phenotypes seen when the flowers are crossed either with themselves or with others.

Methods and Results

The software Aipotu was used for this lab, using the molecular biology tab. The completion of the molecular biology section of this lab did require assistance from the group that completed the genetics portion and the biochemistry portion. They helped provide a list of all different alleles, as well as which alleles are true breeding. The molecular biology tab of this software displays the entire DNA and protein sequence of the alleles and what color pigment they make. The first DNA sequence edited in this experiment was the sequence from the red flower. The base that was edited was from the red sequence, and the base was base #20. It was changed from a G to a C. This led the protein sequence to not be folded, because it did not allow for methionine to be coded, therefore, no pigmented protein could be created, making it a white flower. This led to the discovery that there are multiple ways to create a white flower, because any DNA sequence that does not create a functional pigmented protein will create a white flower (figure 1). Using the knowledge of the different alleles, provided by the genetics group, as well as the biochemistry of a purple allele from the biochemistry group, a purple allele for flowers was created using the molecular biology of the organisms to create a true breeding purple organism (figure 2). The three aromatic amino acids that are responsible for color are phenylalanine, tyrosine, and tryptophan. The red sequence from a purple heterozygote had phenylalanine, and the blue sequence had tyrosine. So an amino acid sequence was created that had both of those amino acids. This was done by changing base 82 of a blue sequence to a U, giving it a phenylalanine.

Figure 1
Figure 2
Specific Tasks

A) There are no differences in the Green DNA sequences in the Green-1 flower. The differences between blue and yellow sequences in Green-2 were at positions 79, and 80. The differences between the red and white sequences in the red flower are at position 7. There were no differences between the white sequences in the white flower. Between every available allele of the colored (non-white) flowers, all of the differences in the DNA sequences fell in bases 79 and 80

  • See figure 3
Figure 3

B) Not all white DNA sequences are the same. When a base was changed on the methionine codon, the protein sequence could not be folded, and the flower turned white. Meaning that whenever a protein sequence fails to be folded, it turns into a white flower, because there is no pigmentations

Figure 4

C) Green-1 was Green and Green. Green-2 was Blue and Yellow. Red was Red and White. White was White and White

  • See figure 4
Figure 5

D) The Purple DNA sequence was created by changing base 82 to a U, adding a phenylalanine to the sequence.

  • See figure 5

E) Certain changes made to the DNA sequences could explain the mutations seen in part one because certain changes to DNA sequences included deletions or insertions, which in some cases was the deletion of methionine, which meant that there was no pigmented protein at all, which led to a white flower. This could also explain some of the mutations in part one that led to a change in color, for they could have changed one of the bases at positions 79 or 80 or they could have changed one of the proteins to one of the aromatic proteins to alter the color of the flower.

Figure 6

F) The protein creates a purple pigmentation.

  • See figure 6

User Page

Assignment Pages

Individual Journal Pages

Class Journal Pages

Retrieved from "https://xmlpipedb.lmucs.org/biodb/spring2024/index.php?title=MSymond1_Week_2&oldid=792"