Introduction of C. elegans ——A model organism Xiaoqi Sang 2011.6.10.

Slides:



Advertisements
Similar presentations
Forward Genetics Phenotype (Function) Genetics Gene A Gene B Gene C Proteins A B C P.
Advertisements

CERISE “C. elegans RNAi space experiment” CERISE “C. elegans RNAi space experiment” RNA interference and protein phosphorylation in space environment using.
Fluorescent proteins Green Fluorescence Protein (GFP) from jellyfish : Revolutionized medical and biological science by providing a way to monitor how.
Rhonda Hummel Why is dying so important? Nobel Prize for Physiology or Medicine 2002 Co-awarded on October 7, 2002 For “genetic regulation of organ development.
Chapter 6 Meiosis.
The Genetics of Caenorthabditis Elegans Brenner, 1974 Lecture by Assaf Tal.
C. elegans lecture Kaveh Ashrafi N412C Genentech Hall
MiRNA in computational biology 1 The Nobel Prize in Physiology or Medicine for 2006 Andrew Z. Fire and Craig C. Mello for their discovery of "RNA interference.
Revisions to the “central dogma” of molecular biology over the last 10 years, scientists have discovered an entirely new category of non-coding RNA genes.
Big lessons from little worms
Advantages of C. elegans: 1. rapid life cycle 2. hermaphrodite
Genetics Lab Dr. Jeff Young Office Hours: BI 412 MR am or by appointment Lecture: T 11 – 11:50 pm in AW410 Lab: WF 1:30 – 3:30.
C. elegans as a model organism
Genetics Genetics. What is Genetics ? Genetics is the study of heredity and variation Examples of genetic variation 1. Domesticated species 2. Human genetics.
Introduction to the Cell Cycle
Lecture 1: Introduction Dr. Mamoun Ahram Faculty of Medicine Second year, Second semester, Principles of Genetics and Molecular Biology.
Fluorescent proteins Green Fluorescence Protein (GFP) from jellyfish : Revolutionized medical and biological science by providng a way to monitor how individual.
Chapter 21 Reading Quiz 1. When cells become specialized in structure & function, it is called … 2. Name 2 of the 5 “model organisms”. 3. What does it.
王歐力 助理教授 Oliver I. Wagner, PhD Assistant Professor National Tsing Hua University Institute of Molecular & Cellular Biology College of Life Science Laboratory.
GFP (Green fluorescent protein) by Kitija Kaulina
Transfection. What is transfection? Broadly defined, transfection is the process of artificially introducing nucleic acids (DNA or RNA) into cells, utilizing.
1 Meiosis and genetic variation. Introduction 2 3 Genes DNA is organized in chromosomes. –Genes have specific places on chromosomes.
Sex Cells Gametes (germ cells) Eggs and Sperm Somatic Cells All other cells Questions: 1, 2, 3, 4.
Regulatory RNAs. Cells produce several types of RNA.
PHONTONICS BIO LASER BY REMINGTON HERNANDEZ. PHONTONICS Photonics covers all technical applications of light over the whole spectrum from ultraviolet.
Caenorhabditis elegans (C. elegans) An elegant worm.
Introduction to C. elegans and RNA interference Why study model organisms?
Welcome! Monday, 1/14 Gametes – sperm and egg are gametes Gene – A section of DNA that codes for a protein Chromosome – Visable DNA Chromatids – two exact.
An Introduction to Model Organisms of Development.
Learning Target: Mitosis v. Meiosis I Can…Compare and contrast key points between the process of mitosis and the process of meiosis to explain why there.
Model Organisms. Model Organism  Important features of all model organisms  Short lifespan  Small, easy and inexpensive to maintain  Produce large.
Asexual and Sexual Reproduction
Caenorhabditis elegans
MiRNA Reading: Lecture notes.
Gas: 2000 liters of methane gas released/day! Size : 6 tons 250kg food eaten every 100kg of elephant dung/day Gestation : 23 months Females give birth.
DO NOW – 2/15/08 Complete the two Dihybrid crosses on eye color and widow’s peak. Report the phenotypic ratios in your DO NOW.
Introduction to C. elegans and RNA interference Why study model organisms?
You have body cells and gametes.
Sydney Brenner by Andrew Brenner. Early Life  Sydney Brenner was born in 1927 in Germinston, South Africa  He discovered the Germinston Public Library.
The Nobel Prize in Physiology or Medicine 2002 Zhou zhe.
Mapping and Characterizing temperature-sensitive, embryonic-lethal
IB404 - Caenorhabditis elegans 1 – Feb 8 1. C. elegans was being studied by a few UK naturalists in the 1960s when South African Sydney Brenner at Cambridge,
Vectors for RNAi.
History of Fluorescent Proteins
Genetics Lab Dr. Jeff Young Office Hours: BI 412 MWT am or by appointment Lecture: T 11 – 11:50 pm in ES410 Lab: WF 1:30 - 4:30.
BIO305 Developmental Biology Instructor: Dave Champlin.
Today’s Goals Describe the advantages of C. elegans as a model organism Discuss the life cycle of the nematode Safely and effectively culture a population.
Introduction to C. elegans Ms. Gaynor Honors Genetics
Learning Target: Mitosis v. Meiosis I Can…Compare and contrast key points between the process of mitosis and the process of meiosis I Will… Describe the.
SECTION 6.1 CHROMOSOMES AND MEIOSIS. YOU HAVE BODY CELLS AND GAMETES  Somatic Cells  Definition: body cells; make up most of your body tissues and organs;
Caenorhabditis elegans. Sydney Brenner ( ) South African biologist (originally chemist) D.Phil from Oxford Extensive work in molecular biology Nobel.
Genetic Basis of Embryonic Development
C. elegans as a model organism
Chapter 13 Meiosis.
Chapter 21 Reading Quiz When cells become specialized in structure & function, it is called … Name 2 of the 5 “model organisms”. What does it mean to be.
RNAi Overview
Introduction to Genetics and Biotechnology
Introduction to Genetics and Biotechnology
Mitosis & Meiosis Lesson 6.
Cellular Division (Mitosis)
Today’s Goals Describe the advantages of C. elegans as a model organism Discuss the life cycle of the nematode Safely and effectively culture a population.
2. 2 Life as a worm-- the nematode C. elegans.
Model organisms: C. elegans
Sources of Variation.
Life as a worm-- the nematode C. elegans
Introduction to C. elegans
You have body cells and gametes.
Volume 44, Issue 6, Pages e3 (March 2018)
2d. Know new combinations of alleles may be generated in a zygote through the fusion of male & female gametes (fertilization)‏ 1.
Presentation transcript:

Introduction of C. elegans ——A model organism Xiaoqi Sang

Page  2 Contents A Short History Characters of C.elegans Nobel Prizes for C. elegans C. elegans and Apoptosis Applications of C. elegans

Page  3 Brief Introduction whole name : Caenorhabditis elegans Free-living, non-parasitic, transparent , about 1 mm in length , lives in temperate soil environments Research into the molecular begun in 1974 Extensively used as a model organism

Page  4 A Short History In 1963, Sydney Brenner introduced C. elegans as a model organism for pursuing research in developmental biology and neurology In 1974, Brenner founded that EMS can induction specificity gene mutation of C. elegans Now is widely used in laboratory research

Page  5 Characters of C. elegans small (about 1 mm in length) Feeds on bacteria Easily to housed and cultivated in large numbers Transparent Easily to manipulation and observation Life cycle is short Have 1090 somatic cells at most Easily to mutagism Can be long-term storage Genome is completely sequenced Nice model organism!

Page  6 C. elegans

Page  7 C. elegans

Page  8 Life Cycle  From egg to egg takes about 3 days  Life span is around 2 to 3 weeks under suitable living condition  Once lay approximately eggs

Page  9 Life Cycle

Page  10 Genome The genome was completely sequenced in 1998, It is the first multicellular-organism (animal) that has a completely sequenced genome The genome size of C. elegans is about a hundred million base pairs Five pairs of autosomes and one pair of sex chromosome Contains approximately 20,100 protein-coding genes Contain more than 16,000 RNA genes

Page  11 Sexual determination C. elegans has two sexes: hermaphrodites and males In nature, hermaphrodites are the most common sex, just 0.05% is males Hermaphrodites can self-fertilize or mate with males but cannot fertilize each other sex determined by the ratio of sex chromosome XX hermaphrodite XO male

Page  12 Applications of C. elegans Cellular differentiation Nervous system Embryo development Cell cycle Meiosis Fertilization Cleavage Fat metabolize RNA Interference (RNAi) Study and memory Aging Apoptosis

Page  13 Nobel Prizes for C. elegans! The first C. elegans Nobel Prize——The Nobel Prize in Physiology or Medicine 2002 For the dicovery of Apoptosis To Sydney Brenner, H. Robert Horvitz and John E. Sulston A second C. elegans Nobel Prize——The Nobel Prize in Physiology or Medicine 2006 For the discovery of RNA interference - gene silencing by double-stranded RNA To Andrew Z. Fire and Craig C. Mello A third C. elegans Nobel Prize——The Nobel Prize in Chemistry 2008 For the discovery and development of the green fluorescent protein To Osamu Shimomura, Martin Chalfie and Roger Y. Tsien

Page  14 C. elegans and Apoptosis C. elegans hermaphrodites have 1090 somatic cells Mature C. elegans remains 959 cells 131 cells commit suicide by apoptosis 116 of the 131 dying cells are cells of the nervous system and other ectoderm

15 To be continue