A Novel Third Isoform of Zebrafish Cytochrome Oxidase IV Brandon Smith Dr. Nancy Bachman, Faculty Advisor.

Slides:



Advertisements
Similar presentations
Research Techniques Made Simple: Polymerase Chain Reaction
Advertisements

Recombinant DNA Technology
Lab 9. Human Mitochondrial Analysis using PCR and Electrophoresis Major Goals of this Experiment Isolate mitochondrial DNA (mtDNA) from cheek cells and.
Recombinant DNA technology
Gene structure DNA replication. Figure 7.4A Figure 7.5.
Online Counseling Resource YCMOU ELearning Drive… School of Architecture, Science and Technology Yashwantrao Chavan Maharashtra Open University, Nashik.
What Are the Methods and Approaches Used Study Knock-Out Mutations? Elaine Chiu Nancy Phang June 4, 2009.
DNA Laboratory SUNY College at Oneonta Dr. Nancy Bachman.
DNA Technology. Biotechnology The use or alteration of cells or biological molecules for specific applications Transgenics Transgenic “changed genes”
DNA Sequencing and Gene Analysis
Lecture ONE: Foundation Course Genetics Tools of Human Molecular Genetics I.
Protein Synthesis Ordinary Level. Lesson Objectives At the end of this lesson you should be able to 1.Outline the steps in protein synthesis 2.Understand.
Manipulating the Genome: DNA Cloning and Analysis 20.1 – 20.3 Lesson 4.8.
Primers. What is a primer? Primers are oligonucleotides, small pieces of RNA or DNA up to 30 base pairs long (a bigger piece is known as a polynucleotide)
Methods for Gene Activity Analysis By Auni Hovanesian Krista Templeton.
Studying Gene Expression and Function
DNA Technology- Cloning, Libraries, and PCR 17 November, 2003 Text Chapter 20.
TOPICS IN (NANO) BIOTECHNOLOGY Lecture 7 5th May, 2006 PhD Course.
CULTURE INDEPENDENT ANALYSIS OF MICROBIAL COMMUNITIES IN SOIL
Analyzing your clone 1) FISH 2) “Restriction mapping” 3) Southern analysis : DNA 4) Northern analysis: RNA tells size tells which tissues or conditions.
From Haystacks to Needles AP Biology Fall Isolating Genes  Gene library: a collection of bacteria that house different cloned DNA fragments, one.
AP Biology: Chapter 14 DNA Technologies
-The methods section of the course covers chapters 21 and 22, not chapters 20 and 21 -Paper discussion on Tuesday - assignment due at the start of class.
Recombinant DNA Technology……….. BTEC3301. DNA Libraries How do you identify the gene of interest and clone only the DNA sequence you are interested? Read.
How do you identify and clone a gene of interest? Shotgun approach? Is there a better way?
Technological Solutions. In 1977 Sanger et al. were able to work out the complete nucleotide sequence in a virus – (Phage 0X174) This breakthrough allowed.
RNA. ________ are coded DNA instructions that control the ___________ of proteins. Genetic ______________ can be decoded by copying part of the ___________.
Remember the limitations? –You must know the sequence of the primer sites to use PCR –How do you go about sequencing regions of a genome about which you.
NIS - BIOLOGY Lecture 57 – Lecture 58 DNA Technology Ozgur Unal 1.
Expression of the Genome The transcriptome. Decoding the Genetic Information  Information encoded in nucleotide sequences contained in discrete units.
Biotechnology.
Genetics 6: Techniques for Producing and Analyzing DNA.
AP Biology DNA Study Guide. Chapter 16 Molecular Basis of Heredity The structure of DNA The major steps to replication The difference between replication,
Fig Fig Fig Fig Fig
Biotechnology l Introduction l Tools l Process l Applications.
1. 2 VARIANTS OF PCR APPLICATIONS OF PCR MECHANICS OF PCR WHAT IS PCR? PRIMER DESIGN.
Genetic Engineering 1 Lecture 18 Pages
Lecture 18 – Functional Genomics Based on chapter 8 Functional and Comparative Genomics Copyright © 2010 Pearson Education Inc.
Chapter 20: DNA Technology and Genomics - Lots of different techniques - Many used in combination with each other - Uses information from every chapter.
While replication, one strand will form a continuous copy while the other form a series of short “Okazaki” fragments Genetic traits can be transferred.
DNA Technology Ch. 20. The Human Genome The human genome has over 3 billion base pairs 97% does not code for proteins Called “Junk DNA” or “Noncoding.
Chapter 20 DNA Technology and Genomics. Biotechnology is the manipulation of organisms or their components to make useful products. Recombinant DNA is.
Trends in Biotechnology
CATEGORY: EXPERIMENTAL TECHNIQUES Polymerase Chain Reaction (PCR) Tarnjit Khera, University of Bristol, UK Background The polymerase chain reaction (PCR)
PCR Polymerase chain reaction. PCR is a method of amplifying (=copy) a target sequence of DNA.
Chapter 20.  Uses recombinant DNA  DNA formed from two different sources  One source is typically a bacterial plasmid  Isolate plasmid from bacteria.
Gene Expression PowerPoint presentation text copied directly from NJCTL with corrections made as needed. Graphics may have been substituted with a similar.
Topic Cloning and analyzing oxalate degrading enzymes to see if they dissolve kidney stones with Dr. VanWert.
Research Techniques Made Simple: Polymerase Chain Reaction
Part 3 Gene Technology & Medicine
Chapter 7 Recombinant DNA Technology and Genomics
Recombinant DNA Technology I
PCR Polymerase Chain Reaction
COURSE OF MICROBIOLOGY
Workshop on the analysis of microbial sequence data using ARB
Cloning Overview DNA can be cloned into bacterial plasmids for research or commercial applications. The recombinant plasmids can be used as a source of.
Chapter 20: DNA Technology and Genomics
DNA Technology and Genomics
DNA Tools & Biotechnology
Material for Quiz 5: Chapter 8
Chapter 9: Biotechnology and Recombinant DNA
Chapter 20 – DNA Technology and Genomics
Chapter 14 Bioinformatics—the study of a genome
DNA Technology.
The student is expected to: (6H) describe how techniques such as DNA fingerprinting, genetic modifications, and chromosomal analysis are used to study.
CHAPTER 12 DNA Technology and the Human Genome
DNA Tools & Biotechnology
Gene structure DNA replication
Chapter 20: DNA Technology and Genomics
Research Techniques Made Simple: Polymerase Chain Reaction
Presentation transcript:

A Novel Third Isoform of Zebrafish Cytochrome Oxidase IV Brandon Smith Dr. Nancy Bachman, Faculty Advisor

Mitochondria Mitochondria are the energy production sites in the cell. Within the mitochondria, specific complexes of proteins carry out chemical reactions. These chemical reactions eventually lead to the production of ATP.

Role of Cytochrome Oxidase Cytochrome Oxidase (COX) is the last enzyme in the mitochondrial respiratory chain. COX IV is thought to have a regulatory function in energy production. This subunit has a number 2 different isoforms. Mammals have two isoforms for COX IV – a widely expressed form and a lung specific form.

Sequencing the DNA The DNA sequence of the various isoforms reveals their amino acid sequence. Once the amino acid sequence is ascertained, the function may be revealed.

Isolating DNA for Sequencing E. coli bacteria contain cloned DNA of the isoforms that are being studied. In order to retrieve the DNA, the bacterial cells are chemically treated so that they burst. After this, centrifugation and other chemical treatments allow the DNA to be isolated in a pure form for sequencing.

Sequence of isoform 1

Analyzing the Sequence Analyzing a DNA sequence involves an array of computing tools –Basic Local Alignment Search Tool (BLAST) is offered on the NCBI web site to compare sequences to others, which helps determine function relative to that of other sequences. –Contig express is a software program that allows for the assembly of a finished sequence from fragments

Aligning sequences with AlignX software AlignX is a software program that allows a user to compare different sequences.

Comparison of Amino Acid Sequences

Gene Expression Experiments Part of answering the “why are there various isoforms” question is to determine where the various isoforms are expressed. This can be done by using Real Time Polymerase Chain Reaction

Dime tour of RT-PCR PCR uses a template DNA strand, small DNA sequences called primers, and enzymes to produce large quantities of a DNA sequence RT-PCR can use dyes to show the progress of an experiment. It can also use enzymes that allow production of DNA from an RNA template

Determining RNA Quality rRNA Bands 

How we use RT-PCR In order to examine the expression of the various isoforms, we can use samples of zebrafish mRNA with the DNA primers that we developed based on the sequences of the isoforms. The mRNA is first used as a template to produce DNA The cDNA samples can be mixed with each of the primers to amplify the amount of DNA. We are able to indicate this with the using fluorescent dyes.

RT-PCR Output

Melt Curve from Expression Experiment

RT-PCR Results After conducting the RT-PCR, we noticed that there was significant expression of both isoform 1 and isoform 3 in the gills, muscle, and ovary of the zebrafish. We also ran an agarose gel to further examine the amount of DNA produced in this step of the experiment, which backs the results from the RT-PCR reaction

Gel Results from RT-PCR

Conclusions Expression of both isoforms is based primarily in Gill and Ovary Tissue. Muscle tissue seems to only express isoform 3, as shown in the gel. Zebrafish isoform 2 has not been tested; in mammals this isoform is only expressed in lung tissue. The gills show the highest expression for both isoforms. This is the first report of a third isoform for COX IV in vertebrates.