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1 BSCI411, Plant Genetics & Molecular Biology Midterm exam ...

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<strong>BSCI411</strong>, <strong>Plant</strong> <strong>Genetics</strong> & <strong>Molecular</strong> <strong>Biology</strong><br />

<strong>Midterm</strong> <strong>exam</strong>, March 15, 2001<br />

Your Name:________________________ SS#_________________________<br />

1. You are provided with EMS-mutagenized M2 seeds of Arabidopsis. Briefly describe<br />

how you are going to screen for mutants defective in leucine biosynthesis?<br />

2. If you have obtained five such mutants (a1 to a5), how are you going to determine<br />

whether they are recessive or dominant (describe the genetic crosses)?<br />

3. If all five mutants are recessive, you then performed complementation tests to test if<br />

they are allelic (mutation in the same gene) or not allelic. You have obtained<br />

following results from such complementation tests (+: wild-type phenotype in F1,<br />

-: mutant in F1). How many complementation groups are there? How are these five<br />

mutations grouped into different complementation groups?<br />

a1 a2 a3 a4 a5<br />

a1 - + + + -<br />

a2 - - + +<br />

a3 - + +<br />

a4 - +<br />

a5 -<br />

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4. A scientist is studying flower pigment synthesis in petunia. These flowers are usually<br />

dark purple. She has obtained several mutants defective in the pigment biosynthesis<br />

pathway. These mutants are: c1: white flower, p1: red flower; p2; pink flower. She<br />

then tested the epistatic relationship among these mutants by constructing double<br />

mutants. Her results: c1 p1: white, c1 p2: white, p1 p2: pink. Indicate which gene<br />

(C1, P1 or P2) acts first in the pigment biosynthesis pathway, which acts second and<br />

which acts last.<br />

5. Based on the ABC model, describe the floral organ type in each whorl:<br />

Whorls: 1 2 3 4<br />

WT Sepal Petal Stamen Carpel<br />

a mutant:<br />

b muatnt:<br />

c mutant:<br />

bc double mutants:<br />

c mutants carrying a 35S-B transgene:<br />

6. Dr. Franks has mapped a gene named SEUSS to chromosome I of Arabidopsis. He<br />

then try to determine the distance between SEUSS and a chromosome I marker CZ1:<br />

CZ1<br />

SEUSS<br />

seuss was originated in the Ler ecotype and was crossed into a Wild-type plant (Col<br />

ecotype). The F1 progeny of this cross is wild-type in phenotype but is heterozygous for<br />

seuss in genotype. He let the F1 plant self and then isolated DNA from 13 seuss mutant<br />

2


plants in F2. CZ1 primers were used to PCR-amplify the CZ1 locus from 13 individual<br />

seuss mutants. The PCR fragment was then diggested with EcoR1 and then run on a 1%<br />

agarose gel. The following is the image from the gel after electrophoreses:<br />

Ler Col 1 2 3 4 5 6 7 8 9 10 11 12 13<br />

___<br />

___ ___ ___ ___<br />

___ ___ ___ ___ ___ ___<br />

___ ___ ___<br />

___<br />

___<br />

_<br />

___<br />

___<br />

_<br />

___<br />

___<br />

_<br />

a. What type of a marker is CZ1? (RFLP? SSLP? CAPS? SNPs?).<br />

b. What is the distance (in % recombination) between SEUSS and CZ1 ? Show your<br />

work.<br />

7. Following is a sequencing gel. What is the DNA sequence? Label 5’ and 3’.<br />

ddA ddG ddC ddT (added to each sequencing reaction)<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

___<br />

3


8. Indicate differences between following terms. Try to indicate as many difference as<br />

you can (even include advantages/disadvantages, application ect.)<br />

Genomic DNA library vs. cDNA library<br />

Microarray vs. DNA chip<br />

Cis-regulatory elements vs. Trans-acting factors<br />

CAPS vs. RFLP<br />

Promoter vs Enhancer<br />

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