Opening Assignment Day 1 Get a pen or pencil out to take a pretest on the material we will learn this week. Unit6: Reproduction, Cell Division, Genetics, DNA & Protein Synthesis BY MRS. SHAW 6 Characteristics of ALL Living things Made of cells Respond to stimuli Grow and develop Life Need energy Evolve Reproduce 6 Characteristics of ALL Living things Made of cells Reproduce Grow and Develop Respond to stimuli Need energy Evolve Sun – Producers – Consumers - Decomposers Why is reproduction required for the survival of a species? Every living thing has a lifespan – a beginning and an end. If species could not reproduce they would die off or become extinct. Reproduction of species also allows for variations to occur so that organisms can adapt to changes in their environment. Sexual vs. Asexual Reproduction Sexual Reproduction Involves two parent sex Pollination cells that combine to create a zygote. Each parent cell adds 50% of the genetic material to the offspring. Each offspring is genetically unique – except for with identical twins Fertilization Sexual Reproduction continued Advantages Disadvantages Genetic Variation!!! Takes more energy and time. Requires two parents. Asexual Reproduction Involves one parent cell that divides to create a two new daughter cells. Each offspring is genetically identical to the parent cell. Asexual Reproduction continued Advantages Disadvantages Faster No genetic variation!! Only requires one parent, so less energy needed Asexual vs. Sexual Reproduction overview SEXUAL ASEXUAL 2 1 DNA of offspring: unique or identical Unique DNA Identical DNA Advantages Genetic Diversity which leads to increase in chance of survival Faster and requires less energy Disadvantages Takes more time and energy No genetic diversity Parents needed Types of Asexual Reproduction Binary Fission: one cell divides to make two cells found in single celled organisms. (prokaryotes) Budding: an offspring grows out of the body of the parent. Spore: a reproductive cell capable of developing into a new individual if environmental conditions are right. Types of Asexual Reproduction continued Vegetative Reproduction: Production of a new plant from a stem or branch. Regeneration: piece of a parent is detached then grows into a new individual. Fragmentation: An organism breaks up into two or more pieces or fragments. The fragments then grow into new organisms. Mitosis vs. Meiosis MITOSIS = BODY CELLS Used in growth and repair MEIOSIS = SEX CELLS ONLY used to create sex cells Type of asexual reproduction One parent cell divides to make two identical daughter cells with a full set of chromosomes (diploid) NOT the same as sexual reproduction One parent cell divides to make four daughter cells with a half set of chromosomes (haploid) Mitosis vs. Meiosis Meiosis vs. Mitosis overview MEIOSIS Starts with MITOSIS One diploid cell – one cell One diploid cell – one cell with a full set of with a full set of chromosomes chromosomes Cell divisions in process 2 1 Daughter cells produced 4 2 Chromosomes in daughter cells Haploid – half set Diploid – full set production of sex cells – egg or sperm production of body cells for growth and repair Main Use Opening Assignment Day 2 Create a venn diagram to compare and contrast sexual and asexual reproduction. Sexual Asexual Practice Question Some organisms are capable of reproducing asexually through processes such as budding or parthenogenesis. What is an advantage of asexual production for an organism? A. It allows organisms to increase population rapidly. B. It allows haploid cells to unite to produce a zygote. C. It allows for greater genetic diversity within a species. D. It allows crossing over to take place during replication. Practice Problem Sponges are important in aquatic ecology and they are capable of reproducing both sexually and asexually. What is an advantage to a species, such as the sponge, of being able to reproduce sexually? A. Sexual reproduction increases genetic variation within a species. B. Sexual reproduction produces offspring that are genetically identical to the parents. C, Sexual reproduction allows the zygote to have twice the number of chromosomes of the parent. D. Sexual reproduction produces a genetically improved zygote from the mutation of the parents' haploid gametes. Bottom of Form Mitosis Remember that Mitosis is a type of asexual reproduction. Mitosis vocabulary: Interphase: the phase before mitosis begins when the DNA is being replicated. Centromeres: the part of a chromosome that links sister chromatids Cytokinesis: the separation of the daughter cells Vocabulary Chromatin: a loose mass of genetic material composed of DNA and proteins Chromosomes: condensed form of DNA wrapped around proteins Chromatid: Chromatid is the daughter strand of a duplicated chromosome that is joined by a single centromere. Stages of Mitosis PMAT Prophase: Chromatin condenses into chromosomes. Nuclear envelope disappears. Metaphase: Chromosomes align at the equatorial plate Anaphase: Sister chromatids separate, centromeres divide Telophase: Chromatin expands and cytoplasm divides Stages of Meiosis Meiosis has similar phases as mitosis with some exceptions Crossing over occurs in Prophase 1 of Meiosis Cells divide twice through 8 phases and the process results in 4 haploid daughter cells Meiosis ONLY happens to produce sex cells (gametes) Meiosis: Crossing Over In prophase I of meiosis, the replicated homologous pair of chromosomes comes together in the process called synapsis, and sections of the chromosomes are exchanged. You can see that after crossing over, the resultant chromosomes are neither entirely maternal nor entirely paternal, but contain genes from both parents. Synapsis and crossing over occur only in meiosis. Video explanations http://highered.mcgraw- hill.com/sites/0072495855/student_view0/chapter 2/animation__comparison_of_meiosis_and_mitosi s__quiz_1_.html Then show “Unique features of Meiosis”. Practice Problem Mitosis and meiosis are processes that occur in an organism during reproduction. Which of the following is a result of mitosis? A. two identical daughter cells B. four haploid cells that have genetic variation C. uncontrolled cell division in the form of cancer cells D. a single diploid cell that is genetically identical to the parent cell Practice Problem Mitosis and meiosis are both processes involved in reproduction. Which statement correctly compares mitosis and meiosis? A. Mitosis and meiosis both produce genetic variation within their daughter cells. B. Mitosis results in the production of two genetically identical diploid cells and meiosis produces four haploid cells. C. Mitosis and meiosis are both divided into only four distinct phases: prophase, metaphase, anaphase, and interphase. D. Mitosis results in the production of two genetically identical diploid cells and meiosis produces four genetically identical haploid cells. What happens when cells continue to divide? http://www.youtube.com/watch?v=lpAa4TWjHQ4 Opening Assignment Day 3 Create a venn diagram to compare and contrast mitosis and meiosis – use your notes from the last 2 days Mitosis Meiosis Practice Problem A scientist is developing a potential treatment for cancer. She grows cells in hundreds of petri dishes and exposes the dishes to environments that are known to cause cancer. After exposure, the scientist determines that some of the petri dishes have cancer cells. What factor do all the petri dishes that contain cancer cells have in common? A. All the petri dishes with cancer cells have a disrupted cell cycle. B. All the petri dishes with cancer cells have been exposed to tobacco smoke. C. All the petri dishes with cancer cells could be treated successfully if they receive the same treatment. D. All the petri dishes with cancer cells have genetically identical cells that make them susceptible to cancer. Practice Problem If an experimental drug aims to prevent and inhibit the multiplication of cancer cells, which of the following would be the best approach for scientists to take in developing the anticancer drug? A. The drug should focus on stimulating weakened cells to grow and divide. B. The drug should prevent meiosis, but also increase mitosis in the cancer cells. C. The drug should stimulate the cells to continue to divide, but at an increased rate. D. The drug should interrupt the cell cycle and prevent cell division in the cancer cells Bottom of Form Reproductive System The reproductive system is a collection of organs that work together for the purpose of producing a new life. The major organs of the reproductive system include the external genitalia and internal organs, including gonads that produce gamete, which is a cell that fuses with another cell during conception in organisms that reproduce sexually.. The Endocrine system works with the Reproductive system to produce hormones, chemical messengers, that help regulate most normal body functions. Sex & Growth Hormones Large scale body changes how do they work turn genes on start new processes in the body by turning genes on that were lying “dormant” Reproductive hormones Pineal gland Testosterone from testes sperm production & secondary sexual characteristics Estrogen from ovaries egg production, preparing uterus for fertilized egg & secondary sexual characteristics BOTH SEXES HAVE BOTH HORMONES just in different amounts. Males have more testosterone than estrogen and females have more estrogen than testosterone Male reproductive system Sperm production happens in the Testes over 100 million produced per day! ~2.5 million released per drop! Male reproductive system Testes & epididymis sperm production & maturation Glands seminal vesicles, prostate, bulbourethal produce seminal fluid nutrient-rich Male reproductive system Testicles produces sperm & hormones Scrotum sac that holds testicles outside of body Epididymis where sperm mature Vas deferens tubes for sperm to travel from testes to penis Prostate, seminal vesicles, Cowper’s (bulbourethal) glands nutrient rich fluid to feed & protect sperm Spermatozoa are male gametes, which contain haploid DNA. Where are spermatozoa produced? ovaries penis prostate testes Spermatogenesis is the process by which sperm develop and mature. Which of the following sequences correctly describes the anatomical path of spermatozoa from formation to ejaculation? testes, vas deferens, prostate, urethra testes, urethra, prostate, vas deferens prostate, vas deferens, testes, urethra prostate, urethra, testes, vas deferens Sperm cells are mobile and must travel through the female reproductive tract to fertilize an egg. Which of the following structures enables sperm cells to swim? A. cilia B. flagella C. pseudopods D. ribosomes Which of the following is NOT a structure of the male reproductive system? A. fallopian tubes B. seminal vesicles C. urethra D. vas deferens Female reproductive system Female reproductive system Ovaries produces eggs & hormones Uterus nurtures fetus; lining builds up each month Fallopian tubes tubes for eggs to travel from ovaries to uterus Cervix opening to uterus, dilates 10 cm for birthing baby Vagina birth canal for birthing baby Female reproductive system Female hormones FSH & LH released from pituitary stimulates egg development & hormone release peak release = release of egg (ovulation) Estrogen released from ovary cells around developing egg stimulates growth of lining of uterus decreasing levels causes menstruation Progesterone released from “corpus luteum” in ovaries cells that used to take care of developing egg stimulates blood supply to lining of uterus decreasing levels causes menstruation Which of the following statements about reproductive hormones is TRUE? A. Only women produce progesterone. B. Estrogen levels are highest during early pregnancy. C. Reproductive hormones affect only the reproductive system. D. Men and women produce both estrogen and testosterone. In the male reproductive system, gametes are produced in the testicles. Which of the following structures of the female reproductive system has the same function as the testicles? A. cervix B. uterus C. fallopian tubes D. ovaries Fertilization Fertilization is when the sperm becomes implanted into the egg, this happens in the fallopian tube. Fertilization results in the formation of a zygote. The zygote starts performing mitosis to grow and eventually forms a blastocyst. The Blastocyst implants in the uterus where it will get the nourishment it needs to continue maturing and growing. Placenta Food & gases diffuse across blood vessels How does a Fetus develop? Brain and spinal cord start to form first but continue developing throughout pregnancy (1st 5 weeks) Then heart forms and starts beating (week 6) Liver, kidneys, intestines, eyes, and nasal cavities (week 68) (ADD THIS TO NOTES: Week 8 is when the embryo stage ends and the fetal stage begins. Limbs and lymphatic system form around week 8 By week 9 most essential organs have begun to develop. Facial features and teeth form by week 12. After this every organ and system continue to mature and develop. Which of the following sequences correctly describes prenatal development? A. blastocyst implants in uterus, zygote forms, heart begins beating, lungs can breathe air, sex organs become visible B. blastocyst implants in the uterus, zygote forms, heart begins beating, sex organs become visible, lungs can breathe air C. zygote forms, blastocyst implants in the uterus, heart begins beating, sex organs become visible, lungs can breathe air D. zygote forms, blastocyst implants in the uterus, sex organs become visible, heart begins beating, lungs can breathe air Bottom of Form Which of the following correctly describes the function of amniotic fluid as it relates to the development of a human fetus? A. It provides protection and moisture for the fetus. B. It carries blood between the fetus and the mother. C. It is where the first fetal blood cells originate. D. It provides nutrition and oxygen for the fetus. Bottom of Form A normal human gestational period lasts forty weeks. Which of the following explains why the eighth week of gestation is notable? A. The gender of the fetus can be determined. B. The embryo is approximately the size of a lime. C. The embryo stage ends and the fetal stage begins. D. Most organ systems are developed and functional. Human fetal development 4 weeks 7 weeks Human fetal development 10 weeks Human fetal development 12 weeks 20 weeks Human fetal development The fetus just spends much of the 2nd & 3rd trimesters just growing …and doing various flip-turns & kicks inside amniotic fluid Week 20 Human fetal development 24 weeks (6 months; 2nd trimester) fetus is covered with fine, downy hair called lanugo. Its skin is protected by a waxy material called vernix Getting crowded in there!! 32 weeks (8 months) The fetus sleeps 9095% of the day & sometimes experiences REM sleep, an indication of dreaming Birth (36 weeks) Intestine Placenta Umbilical cord Wall of uterus Bladder Cervix Vagina Practice question Folate is a crucial vitamin for proper development of the neural tube, which eventually becomes the brain and spinal cord. Which of the following might explain why neural tube defects occur more frequently than other types of birth defects? A. Folate is rarely found in common foods and must be supplemented. B. Since the nervous system forms so late, defects go undetected by early ultrasounds. C. The neural tube forms in the first three weeks, before most women know they are pregnant. D. The first and second trimesters of pregnancy use most of the mother's folate supply, leaving a limited amount for neural tube formation. Bottom of Form Fetal Development Life’s Greatest Miracle http://www.youtube.com/watch?v=1w9o89KkX2A Skip to 7 min. Sample Item 16 SC.912.L.16.17 Mitosis and meiosis are processes involved in cellular reproduction. Which of the following describes an event that results from mitosis but NOT meiosis? A. two stages of cell division B. replication of cellular genetic material C. daughter cells that are identical to the parent cell D. four daughter cells that are produced from each parent cell Sample Item 15 SC.912.L.16.13 A fertilized egg undergoes several stages before it is successfully implanted. The diagram below shows these stages as the fertilized egg travels through the female human reproductive system. In which of the following structures of the female human reproductive system is the blastocyst implanted during normal human development? A. ovary B. uterus C. vagina D. amniotic sac Opening Assignment – Let’s see what you already know Copy and match the definitions on the left with the terms on the right. ___ 1. genotypes made of the same alleles A. alleles ____ 2. different forms of genes for a single trait ____ 3. gene that is always expressed ____ 4. gene that is expressed only in the homozygous state ____ 5. genotypes made of two different alleles ____ 6. the genetic formula for a trait ____ 7. the physical manifestation of a genotype B. Phenotype C. genotype D. homozygous E. recessive F. heterozygous G. Dominant 8. Which ones are dominant alleles? D e k L N n R S 9. Which ones are recessive alleles? M n d F G r k P More review practice Which combinations are . . . . . . 10. Homozygous dominant? AA Gg KK mm uu Rr TT 11. Homozygous recessive ee Ff HH Oo qq Uu ww 12. Genotypes in which dominant gene must show AA Dd EE ff Jj RR Ss 13. Genotypes in which recessive gene must show aa Gg Ff KK rr Oo Tt Part 2: Genetics – Punnett Squares and Pedigrees How are Heredity and Genetics related? Heredity : the passing of traits from parent to offspring Traits are controlled by Genes. A Gene is a section on a chromosome that has genetic information for ONE trait. How are Heredity and Genetics related? SO what is GENETICS? Genetics: The study of how traits are inherited. Gregor Mendel – the Father of Genetics o First known geneticist and “father of genetics” o Was an Austrian monk and was born in 1822 o Did most of his genetic studies on pea plants What did Mendel learn and how did he learn it? He learned that when he self pollinated a purple flowered pea plant all the offspring had purple flowers. X = X = The same thing happened when he self pollinated a white flower plant – all the offspring were white. What did Mendel learn and how did he learn it? So, next he cross pollinated a purple and white flower plant. All the offspring turned out purple. This led him to believe that purple was a dominant trait over white for these plants. What did Mendel learn and how did he learn it? Next, he self pollinated the “hybrid” purple flower plant and what he found was that about 25% of the time the flowers produced were WHITE! Mendel’s Conclusions 1. He concluded that 2 genetic factors control each inherited trait. 2. He also proposed that when organisms reproduce, each reproductive cell contributes one factor for each trait. What are ALLELES? o Alleles are ONE FORM of a gene (there can be more than one form) o Sex cells have one form of a gene on their chromosomes o Body cells have two forms or ALLELES for a single gene (you got one from Mom and one from Dad) o One may be dominant over another. If this happens, the dominant gene is the one expressed. If not, the recessive trait is expressed. Dominant vs. Recessive Dominant traits Recessive traits An allele that blocks An allele that is another allele. Usually expressed using a CAPITAL letter P = purple flower P X p = Pp Purple Hybrid blocked by another allele. Usually expressed using a LOWERCASE letter p = white flower Genotype vs. Phenotype Genotype is the genetic formula of the two alleles that control the expression of the trait. Pp = the genotype of our offspring Phenotype is the physical appearance of the genotype. Purple flowers is the phenotype of the offspring. Homozygous vs. Heterozygous Homo means SAME Hetero means DIFFERENT Homozygous means 2 Heterozygous means 2 of the same alleles Two dominant capitals or two recessive lowercase: PP or pp different alleles One dominant capital letter and one recessive lowercase letter: Pp More Important Vocabulary P1 = Parent generation F1 = daughter generation or 1st generation of offspring from the P1 generation F2 = daughter generation from the offspring of the F1 generation. Punnett Squares A model used to predict possible genotypes and phenotypes of offspring. P1= AA & aa F1= 100% Aa (genotype) 100% Red feathers (phenotype) Mom’s genotype Dad’s genotype What will all the offspring look like (phenotype)? In guinea pigs, short hair, S, is Let’s Practice Complete the following Punnett squares dominant to long hair, s. a. One guinea pig is Ss and one is ss. according to the directions given. Then, fill in the blanks beside each Punnett square with the correct numbers. Expected genotype and phenotype possibilities: Genotypes: ________________ Phenotypes:________________ In guinea pigs, short hair, S, is Let’s Practice Complete the following Punnett squares dominant to long hair, s. b. Both guinea pigs are heterozygous for short hair. according to the directions given. Then, fill in the blanks beside each Punnett square with the correct numbers. Expected genotype and phenotype possibilities: Genotypes: ________________ Phenotypes:________________ In rabbits, brown fur (F) is Opening Assignment Get your homework out then do the Punnett square problem to the right dominant over white fur (f). A heterozygous brown fur rabbit is crossed with a homozygous white fur rabbit. Draw a punnett square and determine the genotypes and phenotypes of the possible offspring. Practice 1. B= Brown eyes b= blue eyes Mom= Bb Dad= BB What are the eye color possibilities if they chose to have children? Genotypes Phenotypes More practice 1. Curly hair is recessive, and straight hair is dominant. A woman with curly hair marries a man who is homozygous dominant for straight hair. Predict the outcomes for their children. Genotypes Phenotypes Other Patterns of Inheritance Incomplete dominance: when one allele is not completely dominant over another and their expression (phenotype) is a mixture of the two. Example: A black mouse is crossed with a white mouse and the offspring have grey fur. Codominance– existing together. Both alleles are expressed. Example: When you cross a black cat with a brown cat their kittens may have black fur with white spots. Other Patterns of Inheritance cont. Multiple alleles: A gene with more than two alleles. Many genes exist this way. For example: A rabbits coat color is determined by a single gene that has at least four different alleles. Other Patterns of Inheritance cont. Polygenic -0 when traits are controlled by two or more genes. For example: Human skin color is made from a combination of many genes. Other Patterns of Inheritance cont. Sex linked inheritance: The inheritance of a trait (phenotype) that is determined by a gene located on one of the sex chromosomes Some diseases or traits are found on the X or Y chromosome only. So since the male is the only one with a Y chromosome, he is the only one able to give the diseases found on the Y and he will only be able to give it to his male offspring. (because if he has a daughter than he has given his X chromosomes and) Sex linked traits http://www.khanacademy.org/science/biology/here dity-and-genetics/v/sex-linked-traits Sample Item 12 SC.912.L.16.2 Hemophilia is a sex-linked, recessive trait. Which of the following describes the probability of hemophilia in the offspring of a man who does not have hemophilia and a woman who is a heterozygous carrier? A. There is a 25% chance that their sons will have hemophilia. B. There is a 100% chance that their sons will have hemophilia. C. There is a 0% chance that their daughters will have hemophilia. D. There is a 50% chance that their daughters will have hemophilia. Opening Assignment Copy and match the term with the correct definition 1. Polygenic inheritance 2. Codominance 3. Sex linked Inheritance 4. Incomplete dominance A. When both alleles are expressed as a mixture B. When both alleles share dominance and are each expressed C. When a trait is controlled by more than one gene D. When a genetic trait is found on either the X or Y chromosome Draw a Punnett square to figure it out A hairline that comes to a point in the center of the forehead is called a widow's peak. Having a widow's peak is a dominant trait, while having a straight hairline is a recessive trait. Cate, a woman with a widow's peak, has two children with James, a man with a straight hairline like her father. What is the probability that their next child will have a straight hairline? A. B. C. D. 0% 25% 50% 75% Four major blood phenotypes (A, B, AB, and O) are determined by three alleles: A, B, and O. A person with type A has a certain protein on their blood cells' membranes. A person with type B has a different protein appearing on their cells' membranes. Cells from type AB have both proteins, but cells from type O, which is recessive, has neither protein. This example illustrates which of the following phenomena? A. codominance B. complete dominance C. partial dominance D. polygenic inheritance Pedigrees A pedigree shows phenotypes of genetically related family members and can also be used to help determine genotypes. Add this to your notes Draw a Punnett square to figure it out Colorblindness is a recessive, sex-linked trait located on the X chromosome. Gaspar is a colorblind man, and his wife Stephanie is a carrier for colorblindness. If they have a male child, what is the probability that their son will be colorblind? A. B. C. D. 0% 25% 50% 100% What are the possible parent options? There are three alleles for blood type: A, B and O. Types A and B are co-dominant, and O is recessive. Based on phenotypes in the pedigree chart below, what is the genotype of the father, Ricky? A. AA B. AO C. AB D. OO Dihybrid Crosses: While a MONOHYBRID CROSS (Ee X EE) shows the probabilities of what happens when one trait is crossed, a DIHYBRID CROSS shows what happens when two traits are crossed. Dihybrid crosses = crossing 2 traits, fur color and tail length, in a hamster E= brown fur e= white fur F = long tail f = short tail EeFF x eeFf Add this to your notes Draw a dihybrid Punnett square to figure it out A goat that is heterozygous for long hair (Hh) and curved horns (Cc) mates with a goat that is homozygous for short hair (hh) and straight horns (cc). Which of the following genotypes is impossible for their offspring to have? A. HhCc B. HHCc C. hhCc D. hhcc FCAT EXPLORER is due 4/25 !! Remember this program equals 3 separate quiz grades for this semester!! START OVER SPRING BREAK!!!! Fetal Development Life’s Greatest Miracle http://www.youtube.com/watch?v=1w9o89KkX2A Skip to 26.45 min. Opening Assignment Get a pencil out and ready to take a pretest on Part 3 – DNA, RNA & Protein Synthesis. Part 3: DNA What is DNA? DNA or Deoxyribonucleic acid is a type of molecule that determines the traits that an individual inherits It is the blueprint of instructions on how to create proteins and every type of cell in your body. Where is DNA located? In Prokaryotes In Eukaryotes In Prokaryotes the DNA is •In Eukaryotes the DNA is located in the nucleus of the cell in the chromosomes. loosely coiled in the cytoplasm. DNA Structure Function Nucleotide: a molecule DNA’s main function is that consists of a sugar, a phosphate, and a base. Bases: adenine, thymine, guanine, cytosine Double helix structure to provide the instructions for creating proteins. Proteins are the chemicals that aid in cellular processes. DNA Replication Transcription Translation The process of making The process of making mRNA from DNA. Remember mRNA takes the instructions for making a necessary protein to the ribosome. a protein from RNA. This happens in the ribosome. What are Chromosomes? Chromosomes are strands of DNA coiled around proteins. Genes, Alleles, Chromosomes & DNA . . . . How are these terms related? Alleles are singular forms of a gene. (single letter B or b) Genes have two alleles . . . one from each parent. (BB, Bb, or bb) Genes are sections of DNA that provide the instructions for a specific trait. Chromosomes are coils of DNA wrapped around proteins, located in the nucleus of eukaryotic cells. Transcription vs. Translation https://www.youtube.com/watch?v=h3b9ArupXZg Opening Assignment 1. Explain the structure of a DNA molecule. 2. Which nucleotide bases pair together in DNA? 3. Are DNA in prokaryotes different than DNA in eukaryotes? Opening Assignment ANSWER Explain the structure of a DNA molecule. DNA is a double helix structure made up of two rungs of nucleotides each with a 5 carbon sugar, a phosphate group, and a nitrogen base. Which nitrogen bases pair together in DNA? Adenine pairs with Thymine and Cytosine pairs with Guanine DNA differences DNA in Prokaryotes DNA in Eukaryotes DNA in Prokaryotes is less complex and circular in pattern made of a single chromosomes DNA in Eukaryotes is more complex and linear in structure made of a pairs of chromosomes (One side from egg and one from sperm) More on DNA structure The weak hydrogen bonds in between the nitrogen bases make it easy for the double strand to be separated when DNA replication needs to occur. Covalent bonds attach the sugar phosphaste backbone together and are a stronger bond than the hydrogen bonds. DNA to RNA to Protein Remember that DNA is a set of instructions to create proteins. By itself, DNA does not do anything except provide the instructions. The instructions are copied during a process called transcription and carried out of the nucleus by a molecule called Messenger RNA (mRNA). DNA to RNA to Protein mRNA takes the copy to the Cytoplasm and Ribosomes where the instructions will be read in a process called translation and then proteins will be made through a process called protein synthesis. Amino Acids to Protein Molecules Remember that amino acids are the sub- units of proteins! There are 20 different amino acids. Their order in the protein molecule determines its structure and function. Proteins may serve e.g., as enzymes, hormones or structural components of a cell. The final protein molecule may consist of several hundred amino acids linked together according to the instructions encoded in the mRNA. DNA, RNA and Protein Synthesis DNA vs. RNA https://www.youtube.com/watch?v=0Elo-zX1k8M Protein Synthesis https://www.youtube.com/watch?v=h5mJbP23Buo Practice Question #1 Which of the following accurately describes the difference between transcription and translation? In transcription, the genetic code of a DNA molecule is first encoded. Translation is the process of converting the DNA code into code that RNA can use. B. In transcription, an amino acid chain is encoded in a DNA molecule. Translation is the process of turning the amino acids into nucleic acids in an RNA molecule. C. In transcription, the genetic code of a DNA molecule is transferred to a messenger RNA molecule. Translation is the process of creating an amino acid chain using the encoded messenger RNA. D. In transcription, a double helix DNA molecule is split into two separate single strands. Translation is the process of joining each single DNA strand with a single strand of matching RNA. A. The Genetic Code The genetic code is nearly universal, meaning that nearly ALL living organisms use the same genetic code. All organisms encode genes using DNA and RNA. All organisms use the same codon for the same amino acid. All organisms are genetically related to all other organisms. Universal Protein Codon Chart Examples UUA = leucine CCC = proline AGC = serine Opening Assignment – Practice Question #2 The genetic code is universal, and is composed of nucleotide triplets. Which of the following lists the four types of nucleotide bases found in the nucleotide triplets of a single strand of DNA? A. ribose, thymine, glucose, uracil B. adenine, cytosine, guanine, uracil C. adenine, cytosine, guanine, thymine D. adenine, deoxyribose, guanine, ribose Practice Question #3 The genetic code is nearly universal, meaning that almost all organisms use the same genetic code. Which statement does NOT help explain why the genetic code is nearly universal? All organisms encode their genes using DNA or RNA. B. All organisms can grow, respond to stimuli, and reproduce. C. All organisms use the same codon for the same amino acid. D. All organisms are genetically related to all other organisms. A. Practice Question #4 In a family with four children, both parents and three of the children have brown eyes; however, the fourth child's eyes are blue. Given these facts, which of the following statements is false? A. Both parents carry one blue-eye gene and one brown-eye gene. B. The brown-eye gene is dominant and the blue-eye gene is recessive. C. The blue-eyed child has one blue-eye gene and one brown-eye gene. D. It is possible that one of the brown-eyed children has two brown-eye genes. DNA Replication For a new cell to be formed through mitosis, the DNA in the original parent cell needs to be duplicated. This process is called DNA Replication and it happens in the Interphase phase of Mitosis which cells spend 90% of their time in. DNA Replication Summary The process of DNA replication involves the double helix strand unwinding and two new strands are formed to match up to the unwound original parental DNA. DNA Replication Summary Each newly synthesized strand of DNA (daughter strand) is made by the addition of a nucleotide that is complementary to the parent strand of DNA. In this way, DNA replication is semiconservative, meaning that one parent strand is always passed on to the daughter helix of DNA. DNA Replication https://www.youtube.com/watch?v=GcrndR-zdyM DNA Replication main points 1. DNA replication is the process of creating copies of the original DNA from the parent cell to be used in the daughter cells. 2. It starts when the DNA in the parent cell is unwound or the bonds between the nitrogen bases are broken by an enzyme called Helicase. 3. DNA Polymerase is the enzyme that matches up the corresponding base pairs on both sides of the rungs to form two new strands. 4. Each new strand has one side that is from the original parent cell and one new side (Semi-conservative model). Opening Assignment DUE AT 9:40 List two reasons that DNA is copied. 1. 2. Explain how these enzymes are used in the process of DNA Replication. A. Helicase B. DNA Polymerase Transcription vs. Translation Create a venn diagram to compare and contrast the processes of transcription and translation in protein synthesis Transcription Translation Practice Question #3 Which of the following statements describes processes that occur during DNA replication? A. A DNA sequence is read by RNA polymerase, which produces another RNA strand complementary to the first strand. B. Two free-floating single strands of DNA are joined by polymerase. The polymerase finds the point at which the two strands will match up into a double strand C. Messenger RNA are decoded by a ribosome to produce an amino acid chain. In the cell's cytoplasm, transfer RNA join the messenger RNA, forming a polypeptide. D. A double-stranded DNA molecule is unwound into single strands. Polymerase matches the right nucleotides to the single strand so that each forms a double strand of DNA. Today’s Activities Read Biology textbook lesson 13.3 on pages 372-376 Define vocabulary and do workbook pages 201-204 This assignment is due at the beginning of class tomorrow. Opening Assignment What is a mutation? List the three types of mutations and give an example of how they each work. Have your workbook out and ready to be graded pages 201-204 Mutations Mutation is a natural process that changes a DNA sequence. And it is more common than you may think. As a cell copies its DNA before dividing, a "typo" occurs every 100,000 or so nucleotides. That's about 120,000 typos each time one of our cells divides. Mutations Most commonly, a single base is substituted for another. Sometimes a base is deleted or an extra base is added. Fortunately, the cell is able to repair most of these changes. When a DNA change remains unrepaired in a cell that will become an egg or a sperm, it is passed down to offspring. Thanks to mutation, we all have some new variations that were not present in our parents. Mutations People commonly use the terms "mutant" and mutation" to describe something undesirable or broken. But mutation is not always bad. Most DNA changes fall in the large areas of the genome that sit between genes, and usually they have no effect. When variations occur within genes, there is more often a consequence, but even then mutation only rarely causes death or disease. Mutation also generates new variations that can give an individual a survival advantage. And most often, mutation gives rise to variations that are neither good nor bad, just different. Types of Mutations Point mutations are small (but significant) changes often in a single nucleotide base or point in the DNA sequence. 3 types of Point Mutations are Substitution, Insertion, and Deletion. Substitution In a substitution mutation, one base is changed to a different base. For example: In the normal strand ATCGACT A substitution can occur where G is replaced by T ATCTACT Because this only affects the codon of a single amino acid these mutations can either have no effect or a minimal one. Point Mutations Insertions occur when one base is inserted from the DNA sequence. For example: In the normal strand ATCGACTGG An insertion can occur where T is added to the strand ATCTGACTGG Point Mutations Deletions occur when one base is deleted from the DNA sequence. For example: In the normal strand ATCGACTGG A deletion can occur where G is deleted from the strand ATCACTGG Frameshift Mutations Both Insertion and Deletion are also called Frameshift Mutations because they shift the reading frame of the genetic message. By shifting the reading frame they can change every amino acid after the mutation. Amoeba Sisters – Mutations https://www.youtube.com/watch?v=GieZ3pk9YVo