Which of the following sequences best describes the correct (5' – 3') organization of a typical eukaryotic gene? Question 12 options: TSS - TATA box – enhancer - coding sequence – BREd - termination site TATA box – TSS – BREd - coding sequence – termination site – enhancer TATA box – BREd - TSS – operon – termination site – enhancer TATA box – BREd – TSS – coding sequence – termination site - enhancer Enhancer - BREd – TSS – TATA box – coding sequence – termination si

Which of the following sequences best describes the correct (5' – 3') organization of a typical eukaryotic gene? Question 12 options: TSS - TATA box – enhancer - coding sequence – BREd - termination site TATA box – TSS – BREd - coding sequence – termination site – enhancer TATA box – BREd - TSS – operon – termination site – enhancer TATA box – BREd – TSS – coding sequence – termination site - enhancer Enhancer - BREd – TSS – TATA box – coding sequence – termination si

Name: Which of the following sequences best describes the correct (5' – 3')
Uploaded: 2024-03-20T06:42:55.000Z
Channel: Bartleby
Description: Which of the following sequences best describes the correct (5' – 3') organization of a typical eukaryotic gene? Question 12 options: TSS - TATA box – enhancer - coding sequence – BREd - termination site TATA box – TSS – BREd - coding sequence – term

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter9: Gene Expression And Gene Regulation

Section: Chapter Questions

Problem 10QP: The pre-mRNA transcript and protein made by several mutant genes were examined. The results are...

See similar textbooks

Similar questions

Nonfunctional HexA protein is responsible for the autosomal recessive disease Tay Sachs. A patient with Tay Sachs produces a normal amount of full length but non-functional HexA protein. Of the choices below, what is the most likely type of mutation responsible for the disease? a) base substitution in an intron 5' splice site b) frameshift in an exon c) missense in an exon d) base substitution in an enhancer region
Which of the following are the enzymes involved in post-transcriptional modification? Question 50 options: RNA polymerase and spliceosomes none of the options are correct RNA polymerase and poly-A polymerase RNA polymerase, poly-A polymerase, and spliceosomes poly-A polymerase and spliceosomes
Shown below are three genes (gene 1, gene 2, and gene 3) located on the same bacterial chromosome. a) Indicate where on the diagram you would find the following for each gene: Promoter (p1 for gene 1, p2 for gene 2, and p3 for gene 3) Transcription termination site (tts1, tts2, and tts3) Start codon (start1, start2, and start3) Stop codon (stop1, stop2, and stop3) Template strand (ts1, ts2, and ts3), the DNA strand that directs RNA synthesis Be sure to indicate the component on the appropriate molecule (DNA or RNA).
The pre-mRNA transcript and protein made by several mutant genes were examined. The results are given below. Determine where in the gene a likely mutation lies: the promoter region, exon, intron, cap on mRNA, or ribosome binding site. a. normal-length transcript, normal-length nonfunctional protein b. normal-length transcript, no protein made c. normal-length transcript, normal-length mRNA, short nonfunctional protein d. normal-length transcript, longer mRNA, shorter nonfunctional protein e. transcript never made
A mutation in which of the following would still allow RNA polymerase to bind to promoters but would prevent the formation of an open complex? Question 4 options: TFIIB Mediator TFIIH TFIID TBP
You just isolated a mutant in the eukaryotic organism C. elegans (aka the world's coolest model organism) that fails to transcribe your favorite gene. Which of the following region(s) are likely to contain your mutation? (You may choose more than one.) Group of answer choices Rut site -10 consensus sequence Rho protein TATA box Sigma subunit binding site Transcription start site
You see partial sequence of a gene as follows (non template strand shown) ...TATAAA(8nts)GGCCAAGGAGCCGCCATGGAACCTGAAG...AAAAAAAAAAAAA... +1 initiation site is underlined. Is this a prokaryotic or eukaryotic gene? Why? A. Eukaryotic gene because it has poly A tail. B. Prokaryotic gene because it has -10 AT rich region. C. Eukaryotic gene because it has a TATA box. D. Prokaryotic gene because it has the Shine Dalgarno sequence.
In Rho-independent termination of transcription (does NOT need the Rho protein), why does the mRNA fall off" of the template DNA?"Question 16 options: because the polymerase pauses over an AT-rich region of DNA because a helicase protein disrupts the H-bonds in the RNA:DNA hybrid because a stem-loop in the mRNA changes the conformation of the NusA protein because a stop codon is reached
You are teaching a class on the regulation of eukaryotic gene expression. such as the promoter regions, where the RNA polymerase II and transcription factors would bind THERE ARE MULTIPLE ANSWERS THAT YOU CAN CHOOSE From the list given - choose all components that you think are part of a typical eukaryotic gene Group of answer choices A core promoter B 3'UTR C introns D enhancer E coding sequence F mediator protein G PPE H exons I DNA-bending protein J 5'UTR
Choose the best answer. transcriptional bubble in prokaryotes is produced by… Group of answer choices TFIID TFIIH Sigma factor and RNA polymerase TATA-Binding Protein Which polymerase transcribes the coding sequences of mRNAs in eukaryotes? Group of answer choices Poly(A) Polymerase RNA Polymerase I RNA Polymerase II RNA Polymerase III What role does TFIID play in transcription? Group of answer choices TFIID binds to the terminator sequence to stop transcription. TFIID acts as a regulatory kinase and helicase. TFIID prevents RNA polymerase II from associating with non-promoter sequences. TFIID binds to the INR and DPE sequences to distort the promoter sequences.
Which of the following general transcription factors aids polymerase binding in the right direction on promoters? Group of answer choices TFIID TFIIB TFIIA TFIIF
The diagram below shows an imaginary eukaryotic structural gene containing two exons. The exon nucleotides are numbered beginning at the transcription start site and a portion of the intron is not shown to save space: Help Center? transcription start site promoter U STACAGTATAAATGAATTAATTGACGTATGTCAATCGGTAAGT...TCAGGTACT U UUU} Phe UUG} Leu exon 1 3 ATGTCATATTTACTTAATTAACTGCATACAGTTAGCCATTCA...AGTCCATGAATGACTTATGTGCGGTTATTTACTGAT... Second letter C Predict the amino acid sequence of the polypeptide encoded by this structural gene. The genetic code is provided below.

SEE MORE QUESTIONS

Recommended textbooks for you

Human Heredity: Principles and Issues (MindTap Co…

Biology

ISBN:

9781305251052

Author:

Michael Cummings

Publisher:

Cengage Learning

Human Heredity: Principles and Issues (MindTap Co…

Biology

ISBN:

9781305251052

Author:

Michael Cummings

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

GET THE APP

About FAQ Academic Integrity Sitemap Document Sitemap

Contact Bartleby Contact Research (Essays)High School Textbooks Literature Guides Concept Explainers by Subject Essay Help Mobile App

GET THE APP

Privacy

Your CA Privacy Rights

Your NV Privacy Rights

About Ads

Manage My Data

bartleby, a Learneo, Inc. business

	TSS - TATA box – enhancer - coding sequence – BREd - termination site
	TATA box – TSS – BREd - coding sequence – termination site – enhancer
	TATA box – BREd - TSS – operon – termination site – enhancer
	TATA box – BREd – TSS – coding sequence – termination site - enhancer
	Enhancer - BREd – TSS – TATA box – coding sequence – termination site