Overview of Working With Telomeres and Cell Viability

Slides:



Advertisements
Similar presentations
and If this shoelace were a chromosome, then these two protective tips would be its.
Advertisements

TELOMERES Dr. José María Romero Romero. TELOMERES are specialized structures at the end of all eukaryotic chromosomes. contain longthy streches of non-coding.
3 Aging 1950 ’ s – Believed that cultivated cells could grow forever If not, then it was a result of a culturing deficiency – In 1943, a cancer cell.
TELOMERES What are they? Why are they important? Telomere shortening and the end-replication problem Telomerase Telomere hypothesis of aging.
Telomeres and Aging: Is there a connection?. What are telomeres? w Telomeres are… Repetitive DNA sequences at the ends of all human chromosomes They contain.
3 Aging 1950 ’ s – Believed that cultivated cells could grow forever If not, then it was a result of a culturing deficiency – In 1943, a cancer cell.
TELOMERES Dr. José María Romero Romero. TELOMERES are specialized structures at the end of all eukaryotic chromosomes. contain longthy streches of non-coding.
Cancer, Aging and Telomeres How molecular genetic research contributes to a better understanding of cancer and aging in humans.
DNA Transmission 21 Jan, Overview DNA replication is prerequisite to cell division. DNA is replicated by using each strand as template for synthesis.
DNA: Structure and Replication
Proofreading and DNA Repair
Chapter 13 DNA Repair and Chromosome Structure. You Must Know DNA proofreading and packaging.
Relationship between Genotype and Phenotype
Unit 4 - Molecular Genetics DNA Replication Protein Synthesis – Transcription – Translation Cell Cycle.
Concept 16.2: Many proteins work together in DNA replication and repair It has not escaped our notice that the specific pairing we have postulated immediately.
Tumor genetics Minna Thullberg
Cellular Senescence: A Link between Tumor Suppression and Organismal Aging.
Cancer. Regulation of Cell Division Two sets of genes control cell division. –Proto-oncogenes. Code for proteins that promote the cell cycle and prevent.
Telomere Terminal Transferase and its Role in Cancer Brian R. Keppler February 27, 2003.
Figure 16.0 Watson and Crick. Figure 16.0x James Watson.
UNIT IV - DNA & CELL DIVISION. I. INTRODUCTION TO DNA ________________ – All of an organism’s DNA; must be copied prior to cell division __________________.
Chromosomes. By the end of this class you should understand: The structure and function of human chromosomes The purpose of the different types of cell.
AP Biology Discussion Notes Tuesday 1/13/2015. Goals for Today Be able to describe the process of science Be able to understand how many people and who.
The Molecular Basis of Heredity Chapter 16. Learning Target 1 I can explain why researchers originally thought protein was the genetic material.
DNA Replication Replication: The process before a cell divides, it duplicates and copies its DNA. DNA  DNA Remember: Each strand can be used to make.
DNA Replication DNA Replication is a semiconservative process where the new DNA is copied onto a parental (conserved) strand. It takes place with surprising.
Chapter 16 DNA REPLICATION. REVIEW: HISTORY & STRUCTURE.
Chapter 9 MITOSIS Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Cells Tissues Organs Systems Organism ADAPTATIONS Change in size Change in number of cells Change into another type of cell.
Telomerase Targets for Cancer Treatment. The ends of chromosomes DNA polymerase has trouble copying the tips of chromosomes- so why don’t we loose a little.
Lesson Overview Lesson Overview Cell Growth, Division, and Reproduction Prokaryote vs. Eukaryote One starting point Proceeds in opposite directions Attach.
TELOMERES &TELOMERASE 18 th Lecture Gihan E-H Gawish, MSc, PhD Ass. Professor Molecular Genetics and Clinical Biochemistry Molecular Genetics and Clinical.
Part II.
Chromatin Structure and Replication
13 Genetics of Aging 1950 ’ s – Believed that cultivated cells could grow forever If not, then it was a result of a culturing deficiency.
Telomeres Aging and Cancer. Replicating the Ends of DNA Molecules Limitations of DNA polymerase create problems for the linear DNA of eukaryotic chromosomes.
AP Biology Discussion Notes Thursday 2/25/2016. Goals for Today Be able to use our biology knowledge to think about (and make) important decisions. Be.
What about the ends (or telomeres) of linear chromosomes? DNA polymerase/ligase cannot fill gap at end of chromosome after RNA primer is removed. this.
The Molecular Basis of Inheritance
DNA Replication (I) 王之仰.
Aging 1950’s Believed that cultivated cells could grow forever If not, then it was a result of a culturing deficiency In 1943, a cancer cell was grown.
DNA Organization and Aging
AP Biology Discussion Notes
Cell Division The Cell Cycle Cloning.
p53 function and regulation in normal cells and cancer cells
Telomerase reverse transcriptase in the regulation of gene expression
Cell Differentiation The Cell Cycle Cell Cycle Regulation Cancer
Houston, we have a problem!
DNA Replication Lecture #23 Ms. Day Honors Biology.
Enabling Replicative Immortality
Relationship between Genotype and Phenotype
Relationship between Genotype and Phenotype
Cellular Reproduction
Regulating Gene Expression
Control of DNA Replication
DNA: The Molecular Basis of Inheritance
K. Lenhard Rudolph, Daniel Hartmann, Oliver G. Opitz  Gastroenterology 
Approaching TERRA Firma: Genomic Functions of Telomeric Noncoding RNA
Lesson Overview 12.3 DNA Replication.
Chapter 13 DNA Replication.
Chromosome structures
Aging and Survival of Cutaneous Microvasculature
© 2016 Pearson Education, Inc.
Biotechnology Genetic Engineering. Biotechnology Genetic Engineering.
The series of stem cell Season Ⅱ
Figure 16.7 A model for DNA replication: the basic concept (Layer 4)
How to prevent and cure cancer and live forever
DNA: The Molecular Basis of Inheritance
Stem cell Basics.
Relationship between Genotype and Phenotype
Presentation transcript:

Overview of Working With Telomeres and Cell Viability ~Steven Artandi Lab at Stanford Suzie Bartram

Introduction Telomeres are nucleotides that cap the ends of chromosomes Promote Cell viability Promote Chromosomal Stability Shorten with cell division and aging because DNA cannot fully replicate the extreme ends Telomerase is a reverse transcriptase that synthesizes telomere repeats Expression of this will lengthen and stabilize the telomeres...cells can possibly have unlimited proliferation

More Information Stem cells and other self-renewing tissue cells express telomerase Usually downregulated with differentiation Found to be upregulated with some cancers On Stanford, the Artandi lab researches the molecular and cellular mechanisms by which telomeres and telomerase influences stem cell function and cancers Telomeres can switch from a capped, protected state to an uncapped state Process increases as the telomeres become shorter Activates a DNA damage response leading to apoptosis

Ideas...? Some bacteria have linear chromosomes with telomeres on the ends.... Work with the regulation of telomerase in bacteria and then apply it to a eukaryotic organism... even a plant or algae? or just make the bacteria more viable.... Needs more discussion and resources, but example would be to engineer a strain of bacteria that is highly active in expressing telomerase (by inducing this process) and then taking the gene(s) responsible and inserting them into an algae's chromosome and try to get the same results If successful... implications could eventually target human telomeres

Potential Problems/ Difficulties Telomerase can be downregulated with differentiation, so it could be difficult to try to work with rapidly dividing cells and the downregulation of the wanted product. Its regulation changes during different stages of the celll cycle The telomeres of eukaryotic cells replicate by a different function so the process may not transfer directly/at all Any ideas? Questions? http://med.stanford.edu/profiles/frdActionServlet?choiceId=facProfile&fid=3848 http://www.pnas.org/content/104/45/17747 http://www.sci.sdsu.edu/~smaloy/MicrobialGenetics/topics/chroms-genes-prots/chromosomes.html