Key Midterm Exam 2

pdf

School

University of California, Santa Barbara *

*We aren’t endorsed by this school

Course

112

Subject

Biology

Date

Feb 20, 2024

Type

pdf

Pages

8

Uploaded by ribsywhose

Report
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ Do not feel compelled to fill all available space! Write legibly. Answer concisely. There are 13 questions on 6 pages 1. (10 points) Fill in the missing cell/tissue types in the lineage diagram below. 1 point for each correct one Top one fertilized egg, zygote, morula (not blastula since the blastocyst basically is the blastula stage for mouse/human) 1
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ 2. (10 Points) Fill in the missing words The Spemann Mangold Organizer has the ability to… 1. become dorsal mesoderm (notochord) 2. dorsalize the ectoderm into neural ectoderm, which forms the neural tube . 3. initiate the movements of gastrulation 4. induce second body/dorsal fates/extra neural tube when transplanted 2 points for correct each (there are five answers) 3. (6 points) Correct any of the statements below that are false: a) The inner cell mass trophoblast (blastocyst) invades the endometrium (uterine lining) to form the placenta. OR The inner cell mass forms the whole embryo and some extraembryonic tissues. b) Cells of the amniotic ectoderm and embryonic epiblast both derive from the inner cell mass. c) All cells migrating through the primitive streak form only embryonic tissues. False. Those that migrate the furthest form extraembryonic mesoderm. d) All embryonic tissues come from the epiblast layer of the inner cell mass. e) Cells migrating through the primitive streak will form all three of the germ layers the embryonic mesoderm and the embryonic endoderm f) Conjoined twins form when one ICM splits into two . As long as the main point was that the conjoined twins are monozygotic, the answer was marked as correct. 2
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ 4. (6 Points) Briefly describe one of the two models of nodal flow. Nodal flow model: Ciliary vortical motion at the gastrulation node (or equivalent structure) directs extracellular movement of determinants (NVPs) Fling morphogens across the midline Two cilia model: Non-motile cilia act as mechanosensors of flow and transduce signal via unidirectional Ca+ release 3 Points Describe (in one to two sentences) an experiment that provided evidence in support of one of the models. For model 1 Mouse mutants lacking cilia or human mutants with L/R patterning defects (not really an experiment but I would accept it) Or the artificial flow experiment wherein persistaltic pumps created a simulation of cilia and found it was able to reverse the flow Reversed the flow and found the opposite patterning of nodal For Model 2 Observed asymmetric Ca2+ fluxes/flashes/transients 2 points Did the result provide correlative evidence, necessity, and/or sufficiency? Mouse mutants (with absent or altered missing cilia lacked nodal flow and) had L/R patterning defects (necessity) Or the artificial flow experiment wherein persistaltic pumps created a simulation of cilia and found it was able to reverse the flow (sufficiency) Reversed the flow and found the opposite patterning of nodal (same as above, sufficiency) Asymmetric Ca2+ flashes (correlative) 1 point 5. (12 Points) Bianchi et al. investigated the role of Juno as the Izumo receptor in fertilization. Fill in the key conclusions, briefly describe the experiment performed, and identify the experimental finding that supports the conclusion. a) Juno is necessary for sperm/egg binding/fusion? (1 pt) and thus for fusion/fertilization (1 pt) 3
Your preview ends here
Eager to read complete document? Join bartleby learn and gain access to the full version
  • Access to all documents
  • Unlimited textbook solutions
  • 24/7 expert homework help
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ Experiment designed to test this: (2 pts) The experiment is the mouse knockout experiment Finding/ supporting evidence (1 sentence): (2 pts) Juno -/- oocytes do not bind to sperm b) Juno is not sufficient for sperm/egg fusion (2 pts) . Experiment designed to test this: (2 pts) Expressing Juno in tissue cultures and Izumo in other cells and mixing them together. Finding/ supporting evidence (1 sentence): (2 pts) Binding was observed but not fusion Also acceptable: Acrosome-reacted normal sperm did not bind as efficiently to zona-free Juno deficient eggs as wild-type controls (Extended Data Fig. 8) 6. (5 Points) Which experiment provided definitive evidence that it is possible to clone a new organism using the nucleus from a fully differentiated, adult cell in mammals ? Dolly the sheep No description needed for full credit. 7. ( 12 Points- 3 per Q ) The work by Takahashi and Yamanaka (2006) identified transcription factors whose overexpression converts embryonic and adult somatic cells into pluripotent stem cells. a) What criteria did they use to choose the 24 genes that they initially selected as candidates for pluripotency factors? Previous literature, genes known to be required in ES cells, early embryonic development and/or pluripotent cells, transcription factor genes, their own findings, 4
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ previous gene transfection experiments b) To test whether any or all of the genes were sufficient to confer pluripotency, they expressed them in somatic cells such as mouse embryonic fibroblasts or adult tail tip fibroblasts. How did they select for pluripotent cells? The selection was for G418 resistance based on expression of a drug-resistance gene from the promoter of a gene that is normally only expressed in pluripotent ES cells and not in fibroblasts. c) How did they figure out which of the 24 genes were really important? Takahashi and Yamanaka used a process of elimination to determine which of the 24 candidate genes were really important for inducing pluripotency. They tested each gene individually to see if it could induce pluripotency on its own. None of the genes could induce pluripotency on their own, so they took a 24-1 approach and removed them one at a time from the combination of 24. They found that four genes (Oct4, Sox2, Klf4, and c-Myc) were individually necessary and together sufficient to induce pluripotency and that the other genes were not necessary for the process. As long as the student mentioned the (n-1) approach, full credit was given. There had to be a description of the experimental design, not just what they found since the question asks about the HOW. d) List three properties of the cells that confirmed that they were pluripotent. 1) Ability to differentiate into cells from all 3 germ layers (endoderm, mesoderm, & ectoderm). 2) Expression of specific pluripotency markers, such as Oct4 and Nanog. 3) Ability to form teratomas, which are tumors containing cells from all three germ layers. 4) Growth curves an option As well as methylation If students listed properties of the pluripotent cells (aka. 1.immortal / long-lived, 2. Self-renewing, 3. Differentiates into different cell types, etc. ) partial credit was given since this is not what the question was asking about. 8. (5 Points) Order the following events from the earliest (1) to latest (5) in frog development. __ 2 __ fertilization __ 1 __ Vgt mRNA localization __ 4 __ cells begin migrating through the dorsal blastopore lip __ 5 __ neural tube closure __ 3 __ cortical rotation 5
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ 9. (6 Points) Which of the following statements are true / false about the primitive streak? Correct any false statements. a. Similar to the chick embryo, the early human embryo also depends on cell migration through a primitive streak True b. Cell migration through the primitive streak enables the formation of the three germ layers. ___ True OR False- endoderm and mesoderm (cells that give rise to ectoderm do not travel through streak) ___________________________________________________________________ c. There is no primitive streak in frog embryos. True d. Hypoblast cells are replaced by cells that migrate through the primitive streak to form embryonic endoderm. True e. The primitive streak forms at the posterior end of the chick embryo. _________ False _________________________________ 10. (7 points) You are a goat herder and you have one goat that produces 10X more of the finest goat milk than any other goat you have heard of. Her name is Milka. You want to clone her! Fill in the blanks of the steps you need to take. Harvest __oocytes/eggs___________ , remove _ _nucleus_or mitotic spindles_ _______, collect ______ _somatic /adult cells_ _______from Milka, fuse with ________ oocytes/eggs_ ___, grow to _________ __blastocyst__ ___ stage in culture, transfer to _____ womb/uterus __________ of a ________ surrogate/related mother _________. 1 point for each 11. (6 points) Indicate which of the following developmental processes depend on Wnts, BMPs, both or neither: _______ both ________Neural crest specification ___ both (or Wnt) ____A/P patterning in frogs _______ both ________A/P patterning in chick _______ both ________A/P patterning in mammals _______ BMP ________L/R patterning in birds and mammals ____ both (or BMP) ____ D/V patterning in frogs (both is technically best answer but bmp was emphasized in class 1 point for each (½ point if they say both and it was only one or the other, ½ point if they say one or the other and it was both) 6
Your preview ends here
Eager to read complete document? Join bartleby learn and gain access to the full version
  • Access to all documents
  • Unlimited textbook solutions
  • 24/7 expert homework help
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ 12. (10 Points) Which of the following cell types derive from neural crest? ____ X ____Dorsal root ganglia ________Paraxial mesoderm ____ X ____Adrenaline-secreting cells ____ X ____Melanocytes in the head ____ X __Melanocytes in the tail ________Notochord ________Limb mesenchyme ____ X ____Facial mesenchyme _____ X ___Bones in the head ________Bones in the leg 1 Point for each 13. (5 points) Which of the following are properties of the neural crest? ___ X ____ ectoderm ___ X ____ migratory _______ move through the primitive streak _______ totipotent ____ X ___ multipotent 1 point for each 7
MCDB 112 Midterm 1 | 100 points | Name__________________________________ SEAT #_____ 12. (10 Points) Which of the following cell types derive from neural crest? ____T____Schwann cells ____F____Paraxial mesoderm _____T___Adrenal medulla _____T___Melanocytes in the head ___T_____Melanocytes in the tail ____F____Neural tube ____F____Limb mesenchyme ___T_____Facial cartilage ____T____ Nerves around aorta ____F____Bones in the leg 13. (5 points) Which of the following are properties of the neural crest? ____F___ Gives rise to neural plate ____T___ Migratory ___F____ Form from endoderm ___T____ Multipotent ___T____ Form at the border between neural plate and epidermis 8