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Suppose X-rays caused a sequence change in the TATA box of a particular gene's promoter. How would that affect the transcription of the gene? (See Figure17.9)

Short Answer

Expert verified

X-rays can change the pattern of the sequence of the TATA box. Then, the transcription factors do not recognize the TATA box sequences. The transcription process does not take place.

Step by step solution

01

Description of gene and transcription

Gene is the segment that is found in the DNA that codes for a protein. It also carries the genetic information that is transferred from one generation to the other generation.

Transcription is the process of producing mRNA from the DNA.

02

Definition of TATA box and promoter

The core segment present in the promoter is the TATA box. It is the sequence in which there is a repetition of A and T is seen. It is otherwise known as non-coding sequences of the DNA segment.

The promoter is the region in which the RNA polymerase can bind to it and initiate the process of transcription.

03

Effect of X-ray in the TATA box

X-rays can cause a mutation in the DNA segment. The X-ray also mutates the TATA box sequences.

The change in the TATA box sequence causes a problem in recognizing the promoter sequences by the transcription factors. If the transcription process does not recognize the promoter region, then the transcription process does not take place.

Hence, the X-ray mutation of TATA box sequences can stop the process of transcription.

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Most popular questions from this chapter

In eukaryotic cells, transcription cannot begin until

  1. the two DNA strands have completely separated and exposed the promoter.

  2. several transcription factors have bound to the promoter.

  3. the 5โ€™caps are removed from the mRNA

  4. the DNA introns are removed from the mRNA.

Which of the following is not true of RNA processing?

  1. Exons are cut out before mRNA leaves the nucleus.

  2. Nucleotides may be added at both ends of the RNA.

  3. Ribozymes may function in RNA splicing.

  4. RNA splicing can be catalyzed by spliceosomes.

In the sequence logo (bottom, left), the horizontal axis shows the primary sequence of the DNA by nucleotide position. Letters for each base are stacked on top of each other according to their relative frequency at that position among the aligned sequences, with the most common base as largest letter at the top of the stack. The height of each letter represents the relative frequency of that base at that position. (a) In the sequence alignment, count the number of each base at position-9 and order them from the most to least frequent. Compare this to the size and placement of each base -9 in the logo. (b) Do the same for position 0 and 1.

What two processes ensure that the correct amino acid is added to a growing polypeptide chain?

Which of the following mutations would be most likely to have a harmful effect on an organism?

  1. a deletion of three nucleotides near the middle of a gene

  2. a single nucleotide deletion in the middle of an intron

  3. a single nucleotide deletion near the end of the coding sequence

  4. a single nucleotide insertion downstream of, and close to, the start of the coding sequence.

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