Which of the following is the feature of split gene?

Wild type genomic sequence of a portion of a gene and the wild type sequence of portion of the protein gene product. The protein sequence only matches partially. ТАT AAA GGG СGA ССА ССТ GсT AАT GGG АСт тTG AGG Tyr Lys Gly Arg Pro Pro Ala Pro Arg Gln Tyr Trp Note: The five amino acids at the amino end of the WT protein match the coding sequence perfectly, but not the six at the carboxyl end. This is for an obvious reason that you should figure out before starting the problem. One of the difficulties with this problem is that you do not have the DNA sequence for the carboxyl end of the protein, but that should not be a problem! And, so far, there are no mutations; nothing unusual, it is just a normal eukaryotic gene!! A mutant is found that has the following protein sequence in that part of the protein: Tyr Lys Gly Arg Thr Cys Ser Premature Stop. What is the likely mutation? between A12 and C13 insert T. between C13 and C14 insert T. A15 -> del. C13 and C14 -> del. G8 -> T. G20 -> A. T21…

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Which elements are required for DNA to behave as a chromosome in yeast cells: a centromere an autonomous replicating sequence two telomeres Antibiotic selection marker

You are analyzing cells that express a fusion gene encoding a FLAG-tagged protein of interest. Upon amino acid sequence analysis, you find that the FLAG protein sequence aligns to the sequence at the end of the fusion protein sequence you have. Where is the tag sequence located?   Group of answer choices At the 5’ end of the gene and the C-term of your protein of interest At the 5’ end of the gene and the N-term of your protein of interest At the 3’ end of the gene and the C-term of your protein of interest At the 3’ end of the gene and the N-term of your protein of interest

Inability to recognize double stranded DNA breaks results in increases rates of:   Question 20 options:   translocations   fragmented chromosomes   increased rates of nonhomologous end joining   gene deletions   increased rates of homology directed repair

Briefly explain how Genome Wide Association Studies (GWAS) are done. Then, using this example of a Manhattan Plot explain what each of the X-axis and the Y-axis signifies in a GWAS.

An organism no longer needs to express a particular gene. What is one strategy it might use of the methods discussed in class? Select all that apply. 0.000 de-methylate C bases in the genome acetylate C bases in the genome methylate C bases in the genome acetylate histones de-acetylate histones de-acetylate C bases in the genome

Path: p QUESTION 44 What precautions might you take when working in a BSL-2 lab? Is there a risk? T TTArial 3 (12pt) Path: p QUESTION 45 What are insertion and deletion mutations? Why might they be harmful to a cell? Click Save and Submit to save and submit. Click Save All Answers to save all answers. P Type here to search 立

Line A below shows the peptide synthesized after transcription and translation of a piece of DNA.  Line B shows the peptide synthesized after a mutation in this piece of DNA. proline- arginine - aspartic acid - lysine - glycine proline - glutamine - aspartic acid - lysine — glycine The type of change in the DNA most likely to be responsible for the difference between the peptides is:   a. A frame-shift mutation d. A base deletion b. A base insertion e. A silent mutation f. A base substitution