Heredity B
Re: Heredity B
We were going through a test in class and came across a question that everyone got wrong. We don't agree with the answer key but wanted to know if anyone understands why the answer could possibly be that. If you know why or also disagree with the answer key please share your opinion.
The question is:
Given this mRNA code and the above chart, what amino acid sequence will be produced. For the diagram use the amino acid coding chart.
GGTUAAUGGUGAAGUCACCCCCCUGUGAACAAAUC
The answer key says the answer is supposed to be:
Meth, Val, Lys, Cys, Thr, Pro, Leu, Stop
We got:
Pro, Ile, Thr, Thr, Ser, Arg, Gly, Gly, Thr, Leu, Val, Stop
The question is:
Given this mRNA code and the above chart, what amino acid sequence will be produced. For the diagram use the amino acid coding chart.
GGTUAAUGGUGAAGUCACCCCCCUGUGAACAAAUC
The answer key says the answer is supposed to be:
Meth, Val, Lys, Cys, Thr, Pro, Leu, Stop
We got:
Pro, Ile, Thr, Thr, Ser, Arg, Gly, Gly, Thr, Leu, Val, Stop
Re: Heredity B
Remember that AUG (bolded above) is the codon that initiates translation, so the protein would start with Methionine and move on until the stop codon.TikaKK wrote: ↑Sat Nov 09, 2019 8:37 am We were going through a test in class and came across a question that everyone got wrong. We don't agree with the answer key but wanted to know if anyone understands why the answer could possibly be that. If you know why or also disagree with the answer key please share your opinion.
The question is:
Given this mRNA code and the above chart, what amino acid sequence will be produced. For the diagram use the amino acid coding chart.
GGTUAAUGGUGAAGUCACCCCCCUGUGAACAAAUC
The answer key says the answer is supposed to be:
Meth, Val, Lys, Cys, Thr, Pro, Leu, Stop
We got:
Pro, Ile, Thr, Thr, Ser, Arg, Gly, Gly, Thr, Leu, Val, Stop
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Re: Heredity B
How much do we have to know about protein synthesis for this event?
COMPS (Mira Loma, Christensen, Regs, States [nvm]):
Mission Possible 4-8-1 (send golf balls pls)
Game On 8-1-1
Heredity 4-2-2
Current ~ Mission Possible, Heredity, Game On
Send golf balls
Mission Possible 4-8-1 (send golf balls pls)
Game On 8-1-1
Heredity 4-2-2
Current ~ Mission Possible, Heredity, Game On
Send golf balls
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Re: Heredity B
What are some common tiebreakers for this event? Are most tiebreakers time or some questions?
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Re: Heredity B
State & Regional 2019 events B
Solar system, Water Quality, Anatomy and Physiology- 1st State & Regional
Heredity 4th state, 2nd regional 




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Re: Heredity B
So, my partner and I were taking a test, and we came across this question:
37. Suppose the trait of dimples runs in a family line. John, a male with dimples marries Mary, a female
that’s younger than John and has no dimples. Both heterozygotes, that have 4 children, (listed youngest to
oldest), Lucy, an unaffected female; Andy, a male with dimples; Jordan, an unaffected male; and
Veronica, a female with no dimples. The 2nd oldest out of the 4 siblings marries a younger, unaffected
female, and has 3 daughters, the youngest with dimples. The youngest out of the 4 siblings marries a
younger male called Jake, who doesn’t know whether or not he has dimples. Jake's parents, listed from
birth date, are Jeff, with no dimples, and Amy, with dimples. Jake and the youngest of the 4 siblings have
3 unaffected children, the oldest and youngest are sons, and the middle being a daughter.
a. Construct a pedigree for this situation.
b. What type of inheritance is shown?
We were confused when we saw this question because, in the question, it states that John and Mary are both heterozygotes, but John has dimples and Mary doesn't. That didn't make much sense to us. We assumed that John was affected and Mary wasn't, and we drew the pedigree. Looking at the pedigree that we drew, it looked like it was autosomal recessive (equal amounts of girls & boys affected and skips generations), but the key said it was autosomal dominant. When we looked at the key, we noticed that Jordan was marked as affected in the pedigree while in the problem, he was described as being unaffected.
Can anybody please explain what we had done wrong?
37. Suppose the trait of dimples runs in a family line. John, a male with dimples marries Mary, a female
that’s younger than John and has no dimples. Both heterozygotes, that have 4 children, (listed youngest to
oldest), Lucy, an unaffected female; Andy, a male with dimples; Jordan, an unaffected male; and
Veronica, a female with no dimples. The 2nd oldest out of the 4 siblings marries a younger, unaffected
female, and has 3 daughters, the youngest with dimples. The youngest out of the 4 siblings marries a
younger male called Jake, who doesn’t know whether or not he has dimples. Jake's parents, listed from
birth date, are Jeff, with no dimples, and Amy, with dimples. Jake and the youngest of the 4 siblings have
3 unaffected children, the oldest and youngest are sons, and the middle being a daughter.
a. Construct a pedigree for this situation.
b. What type of inheritance is shown?
We were confused when we saw this question because, in the question, it states that John and Mary are both heterozygotes, but John has dimples and Mary doesn't. That didn't make much sense to us. We assumed that John was affected and Mary wasn't, and we drew the pedigree. Looking at the pedigree that we drew, it looked like it was autosomal recessive (equal amounts of girls & boys affected and skips generations), but the key said it was autosomal dominant. When we looked at the key, we noticed that Jordan was marked as affected in the pedigree while in the problem, he was described as being unaffected.
Can anybody please explain what we had done wrong?
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Re: Heredity B
reninkidney wrote: ↑Thu Dec 26, 2019 6:24 pm So, my partner and I were taking a test, and we came across this question:
37. Suppose the trait of dimples runs in a family line. John, a male with dimples marries Mary, a female
that’s younger than John and has no dimples. Both heterozygotes, that have 4 children, (listed youngest to
oldest), Lucy, an unaffected female; Andy, a male with dimples; Jordan, an unaffected male; and
Veronica, a female with no dimples. The 2nd oldest out of the 4 siblings marries a younger, unaffected
female, and has 3 daughters, the youngest with dimples. The youngest out of the 4 siblings marries a
younger male called Jake, who doesn’t know whether or not he has dimples. Jake's parents, listed from
birth date, are Jeff, with no dimples, and Amy, with dimples. Jake and the youngest of the 4 siblings have
3 unaffected children, the oldest and youngest are sons, and the middle being a daughter.
a. Construct a pedigree for this situation.
b. What type of inheritance is shown?
We were confused when we saw this question because, in the question, it states that John and Mary are both heterozygotes, but John has dimples and Mary doesn't. That didn't make much sense to us. We assumed that John was affected and Mary wasn't, and we drew the pedigree. Looking at the pedigree that we drew, it looked like it was autosomal recessive (equal amounts of girls & boys affected and skips generations), but the key said it was autosomal dominant. When we looked at the key, we noticed that Jordan was marked as affected in the pedigree while in the problem, he was described as being unaffected.
Can anybody please explain what we had done wrong?
Don't worry! You were right in constructing the pedigree. The pedigree described in the test and key do not match up, and many people's genotypes are ambiguous. I definitely made mistakes when writing this question and the key, and I apologize if this caused any confusion

Thanks for catching that mistake, I always post errata (and other tests) on my wiki page: https://scioly.org/wiki/index.php/User:Mr.Epithelium
My first name is Nonkeratinized. My middle name is Squamous.
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Re: Heredity B
No problem. Thanks for taking the time to go back and check!Mr.Epithelium wrote: ↑Thu Dec 26, 2019 8:08 pmreninkidney wrote: ↑Thu Dec 26, 2019 6:24 pm So, my partner and I were taking a test, and we came across this question:
37. Suppose the trait of dimples runs in a family line. John, a male with dimples marries Mary, a female
that’s younger than John and has no dimples. Both heterozygotes, that have 4 children, (listed youngest to
oldest), Lucy, an unaffected female; Andy, a male with dimples; Jordan, an unaffected male; and
Veronica, a female with no dimples. The 2nd oldest out of the 4 siblings marries a younger, unaffected
female, and has 3 daughters, the youngest with dimples. The youngest out of the 4 siblings marries a
younger male called Jake, who doesn’t know whether or not he has dimples. Jake's parents, listed from
birth date, are Jeff, with no dimples, and Amy, with dimples. Jake and the youngest of the 4 siblings have
3 unaffected children, the oldest and youngest are sons, and the middle being a daughter.
a. Construct a pedigree for this situation.
b. What type of inheritance is shown?
We were confused when we saw this question because, in the question, it states that John and Mary are both heterozygotes, but John has dimples and Mary doesn't. That didn't make much sense to us. We assumed that John was affected and Mary wasn't, and we drew the pedigree. Looking at the pedigree that we drew, it looked like it was autosomal recessive (equal amounts of girls & boys affected and skips generations), but the key said it was autosomal dominant. When we looked at the key, we noticed that Jordan was marked as affected in the pedigree while in the problem, he was described as being unaffected.
Can anybody please explain what we had done wrong?
Don't worry! You were right in constructing the pedigree. The pedigree described in the test and key do not match up, and many people's genotypes are ambiguous. I definitely made mistakes when writing this question and the key, and I apologize if this caused any confusion.
Thanks for catching that mistake, I always post errata (and other tests) on my wiki page: https://scioly.org/wiki/index.php/User:Mr.Epithelium
2021 Events: A&P, Heredity, XPD