* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Ironing Out Jesse`s Problem
Frameshift mutation wikipedia , lookup
Site-specific recombinase technology wikipedia , lookup
Cre-Lox recombination wikipedia , lookup
Nutriepigenomics wikipedia , lookup
Public health genomics wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Nucleic acid analogue wikipedia , lookup
Non-coding DNA wikipedia , lookup
Genetic engineering wikipedia , lookup
Designer baby wikipedia , lookup
Genome editing wikipedia , lookup
Genome (book) wikipedia , lookup
History of genetic engineering wikipedia , lookup
Therapeutic gene modulation wikipedia , lookup
Helitron (biology) wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Microevolution wikipedia , lookup
Expanded genetic code wikipedia , lookup
Certificate of Initial Mastery Task Booklet 2011-2012 School Year Students’ Task Guide Ironing Out Jesse’s Problem Science--Biology On-Demand Task 4.1.02 Section 3. The Standards and Grade Span Expectations Assessed by this Task RIDE Applied Learning RIDE Applied Learning Critical thinking, in which the student detects incompleteness, inconsistency, and opportunities for expansion of ideas, products, procedures, etc. and formulates core questions and assertions about topics or areas of interest. (DOK-3) Problem solving, in which the student organizes and conducts a process to create intellectual or physical products, hold an event, conduct a process, or otherwise move towards the solution of an identified issue or problem. (DOK-3) Communication, in which the student questions, informs, and learns from others. (DOK-3) Science GSEs LS1 (9-11) – 2a, 2b and 2c - Understanding of the molecular basis for heredity LS3 (9-11) -7 – understanding of Natural Selection/evolution by investigating how the sorting and recombination of genes in sexual reproduction results in a great variety of possible gene combinations in the offspring of any two parents. Math CCSS Common Core: Math - Statistics and Probability: S-MD7. (+) Analyze decisions and strategies using probability concepts (e.g., product testing, medical testing, pulling a hockey goalie at the end of a game) Academic Expectations 2.2PS Collecting, interpreting, organizing, analyzing and utilizing data to arrive at effective solutions relevant to the real world Applied Learning Standard – Problem Solving 2 Altered by Warwick Science Proficiency Committee Section 5. Task Criteria This list of criteria describes what your students need to do in order to meet standard on this task. You should explain each expectation in the Meets Standard column. Be sure all your students understand what each expectation means before you give your class this task. In order to meet standard on this task, a students cannot get a “zero” on any expectation in this task. When you discuss these criteria with your class, ask them to use the right hand column to take notes, write down hints to themselves, record points that seem important to them or things that they don’t want to forget. Expectations Meets Standard 3 Determine the experimental or theoretical probability of an event in a problem-solving situation and express the result as a fraction, decimal, or percent. Student correctly determines the answer and expresses it in a fraction, decimal, or percent. OR Student correctly determines the answer and expresses it in a fraction, decimal, or percent but bases it on incorrect evidence. S-MD7 Question 1a (DOK 2) Explain how the sorting and recombination of genes in sexual reproduction results in a great variety of possible gene combinations in the offspring of any two parents. (e.g. manipulate models to represent and predict genotypes and phenotypes, Punnett Squares, probability activities). S-MD7 Student correctly relates genetic inheritance and probability to Mendel’s Law of Segregation. Minor errors do not detract from meaning. Written description demonstrates a connection to the Punnett Square work. LS3 (9-11)-7b LS3 (9-11)-7b Question 1b (DOK 3) Determine how genetic information in DNA molecules provides instructions for assembling protein molecules. Understand that the code used is virtually the same for all life forms. LS1 (9-11)-2a, 2b and 2 c Question 2a (DOK 3) Question 2b (DOK 3) Question 3b (DOK 3) 3 Student determines the amino acid sequences for both segments allowing for 1-2 mistakes. AND Student accurately describes transcription and translation in the cell in writing and/or labeled diagrams. Minor errors do not detract from meaning. LS1 (9-11)-2a and c Student Notes: Section 5. Task Criteria Expectations Explain how DNA may be altered and how this affects genes/heredity. LS1 (9-11)-2b Meets Standard 3 Student correctly identifies the specific difference between the normal segment and the diseasecausing segment of the amino acid sequences. AND Describes an accurate mechanism by which the genetic change could have occurred. Minor errors do not detract from meaning. Question 3a (DOK 3) Explain how DNA may be altered and how this affects genes/heredity. LS1 (9-11)-2b Student explains the impact of amino acid sequence changes on the function of proteins. Minor errors do not detract from meaning LS1 (9-11)-2b Question 3b (DOK 3) Demonstrates an understanding of the molecular basis for heredity by explaining how DNA may be altered and how this effect genes/heredity. LS1 (9-11)-2b A.E. 2.2 AL Problem Solving Question 4 (DOK 3) 4 LS1 (9-11)-2b Student correctly describes and cites examples for the occurrence of the Hemoglobin disorder. LS1 (9-11)-2b A.E. 2.2 AL Problem Solving Student Notes: Section 6. Background Information Jesse has been diagnosed with hereditary Hemoglobin disorder, a genetic disease caused by a mutated gene that results in a serious medical condition. This condition causes his body to absorb too much iron in the pancreas, liver and skin. Without treatment, the iron deposits can damage these organs. His parents do not have the Hemoglobin disorder and do not understand anything about the disease or its causes. They are considering having another child and are concerned that their next child could also have the Hemoglobin disorder. As a genetic counselor you have access to diagrams of the normal gene, the mutated Hemoglobin gene sequence, and the genetic code chart so that you can show and explain to Jesse’s parents exactly how Jesse got the inherited disease and the probability of it occurring in future offspring. Task Prompt As a genetic counselor, you will use the data from your research (punnet squares, amino acid sequencing, Mendel’s Law of Segregation, transcription, translation, mutations, hemoglobin protein) to explain to Jesse’s parents how he got the hemoglobin disease. You will also use the data to discuss the probability of their future children inheriting the same disorder. (You will do so by answering questions 1-4) 5 Altered by Warwick Science Proficiency Committee 6 Altered by Warwick Science Proficiency Committee 1a. Given the information in the prompt, determine the probability that Jesse’s parents will have another child with Hemoglobin disorder. Using a Punnett Square. Punnet Square: Probability (report your answer as a fraction, decimal or percent): 1b. Using the information from problem 1a and what you know about Jesse and his parents, explain how Jesse inherited the Hemoglobin disorder in terms of Mendel’s Law of Segregation. Diagrams may be used to enhance your answer. 7 Altered by Warwick Science Proficiency Committee 2a. List the corresponding amino acid sequences that result from each of the small segments of DNA within the Hemoglobin gene shown below (NOTE: one side of the DNA double helix is shown). A genetic code table has been provided in the prompt. Normal DNA sequence T C T - A T A - T G C -A C G- G T C - C A C- C T C Amino Acid Sequence: __________________________________________________________________________________ Jesse’s DNA sequence T C T - A T A- T G C -A T G- G T C- C A C- C T C Amino Acid Sequence: __________________________________________________________________________________ 2b. Describe how the transcription AND translation of Jesse’s sequence would occur in the cell. You may include labeled diagrams in your answer. 8 Altered by Warwick Science Proficiency Committee 3a. Identify and indicate the specific mutation between the normal sequence and Jesse’s sequence of amino acids. Explain how the mutation might have occurred in the DNA. (Refer to Question 2a) 3b. Explain why changing Jesse’s amino acid sequence affected the function of Jesse’s hemoglobin protein. 9 Altered by Warwick Science Proficiency Committee 4. Mutations occur naturally 1% of the time. As a genetic counselor you have analyzed all of the data relating to Jessie’s hemoglobin disorder. It is your job to consult with his parents regarding your findings. Include in your report the probability of their future children being affected by the disorder. Be sure to explain the effect on the amino acid sequence, and the function of that protein. 10 Altered by Warwick Science Proficiency Committee Section 7. Task Rubric: Ironing Out Jesse’s Problem Scorer 1 This rubric explains the elements of the prompt and standards that should be included in the work. To achieve a successful score on this task, a student must MEET or EXCEED standard on any expectation with an asterisk. In order to meet standard on this task, a students cannot get a “zero” on any expectation in this task. Expectations Exceeds standard 4 Meets standard 3 Determine the experimental or theoretical probability of an event in a problem-solving situation and express the result as a fraction, decimal, or percent. S-MD7 Question 1a (DOK 2) Student correctly determines the probability and expresses it in a fraction, decimal, or percent. AND All evidence is accurately shown. Student correctly determines the answer and expresses it in a fraction, decimal, or percent. OR Student correctly determines the answer and expresses it in a fraction, decimal, or percent but bases it on incorrect evidence. S-MD7 Explain how the sorting and recombination of genes in sexual reproduction results in a great variety of possible gene combinations in the offspring of any two parents. (e.g. manipulate models to represent and predict genotypes and phenotypes, Punnett Squares, probability activities). LS3 (9-11)-7b Question 1b (DOK 3) Student thoroughly relates genetic inheritance and probability to Mendel’s Law of Segregation. Detailed written or diagrammed descriptions of Mendel’s Law and demonstrate a clear connection to the Punnett Square work. Appropriate vocabulary is used. Student correctly relates genetic inheritance and probability to Mendel’s Law of Segregation. Minor errors do not detract from meaning. Written description demonstrates a connection to the Punnett Square work. LS3 (9-11)-7b Student relates genetic inheritance and probability to Mendel’s Law of Segregation. Student does not relate the description to the Punnett square. Student does not relate connections between genetic inheritance and probability to Mendel’s Law of Segregation. Major misconceptions are apparent in the explanation. Determine how genetic information in DNA molecules provides instructions for assembling protein molecules. Understand that the code used is virtually the same for all life forms.LS1 (9-11)-2a and c Question 2a (DOK 1) Question 2b (DOK 2) Student determines the correct amino acid sequences for both segments of DNA. AND Student thoroughly describes transcription and translation in the cell in writing and/ or thoroughly labeled diagrams. Appropriate vocabulary is used. Student determines the amino acid sequences for both segments allowing for 1-2 mistakes. AND Student accurately describes transcription and translation in the cell in writing and/or labeled diagrams. Minor errors do not detract from meaning. LS1 (9-11)-2a and c Student determines the amino acid sequences for both segments of DNA allowing for 3-4 mistakes AND Student accurately describes transcription and/or translation in writing and/or labeled diagrams. Minor errors do not detract from meaning. Student is unable to determine the correct amino acid sequences. AND The student incorrectly describes the processes by which amino acids are determined. Explain how DNA may be altered and how this affects genes/heredity. LS1 (9-11)-2b Question 3a (DOK 3) Question 3b (DOK 3) Student correctly identifies the specific difference between the normal segment and the disease-causing segment of amino acid sequences. AND Describes an accurate mechanism by which the genetic change could have occurred using appropriate vocabulary to thoroughly describe the mechanism AND how it affects the function of the protein. Student correctly describes and correctly analyzes the relationship between the change in amino acid sequence which results in a new protein. Student also describes the probability of any future children inheriting the disease. Student uses proper vocabulary terms. Student correctly identifies the specific difference between the normal segment and the disease-causing segment of the amino acid sequences. AND Describes an accurate mechanism by which the genetic change could have occurred. Minor errors do not detract from meaning. And how it affects the function of the protein. LS1 (9-11)-2b Student identifies a difference between the normal and the disease-causing segment of the amino acid sequences. AND Describes a cause of the change that does not necessarily include a mechanism by which the change occurred. AND incorrectly describes how it affects the function of the protein. Student identifies the relationship between the change in amino acid sequence but fails to understand the correlation. Student incorrectly identifies a difference between the normal and disease-causing segment of amino acid sequences. AND No description of a cause or mechanism for the change is included. AND incorrectly describes how it affects the function of the protein. Demonstrates and understanding of the molecular basis for heredity by explaining how DNA may be altered and how this effect genes/heredity. LS1 (9-11)-2b A.E. 2.2 AL Problem Solving Question 4 (DOK 3) Student correctly describes and correctly analyses the relationship between the change in amino acid sequence which results in a new protein. Student also describes the probability of any future children inheriting the disease. Minor errors do not detract from meaning. LS1 (9-11)-2b, A.E. 2.2 AL Problem Solving Nearly meets standard 2 Student determines an incorrect answer, but the answer correctly corresponds to the evidence provided by the student. Below standard 1 Student shows little to no knowledge of how to determine genetic probability. Student attempts to describe the connection between amino acid sequence and protein function. Comments _______________________________________________________________________________________________________________________ Score ______________ Scorer’s Initials ______________ 11 Altered by Warwick Science Proficiency Committee 0