Place the steps below in the correct order as they would occur within a signal transduction pathway. Drag and drop options into correct order and submit. For keyboard navigation... SHOW MORE V An inactive signal transduction molecule is activated. A transcription factor enters the nucleus. An active signal transduction molecule binds a transcription factor. A gene is expressed. A receptor undergoes a conformational change. A ligand binds to a receptor. II II II II II II

Place the steps below in the correct order as they would occur within a signal transduction pathway. Drag and drop options into correct order and submit. For keyboard navigation... SHOW MORE V An inactive signal transduction molecule is activated. A transcription factor enters the nucleus. An active signal transduction molecule binds a transcription factor. A gene is expressed. A receptor undergoes a conformational change. A ligand binds to a receptor. II II II II II II

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Description: Place the steps below in the correct order as they would occur within a signaltransduction pathway.Drag and drop options into correct order and submit. For keyboard navigation...SHOW MORE ♥An inactive signal transduction molecule is activated.A tran

Biology 2e

2nd Edition

ISBN:9781947172517

Author:Matthew Douglas, Jung Choi, Mary Ann Clark

Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark

Chapter9: Cell Communication

Section: Chapter Questions

Problem 1VCQ: Figure 9.8 HER2 is a receptor tyrosine kinase. In 30 percent of human breast cancers, HER2 is...

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which of the following correctly describes how protein kinase A can activate genes? A: nuclear protein kinase A is activated by cAMP to phosphorylate general transcription factors B: cytosolic protein kinase A is activated by cAMP to release the catalytic subunits, which move into the nucleus and phosphorylate CREB C: cytosolic protein kinase A is activated by cAMP to release the catalytic subunits, which move into the nucleus and phosphorylate general transcription factors D: G protein-coupled receptors may be desensitized by serine phosphorylation
Outline the general features of a signal transduction pathwaystarting with binding of a PAMP by a membrane-associated PRR.
Two protein kinases, barley kinase and hops kinase, function sequentially in an intracellular signaling pathway. If either kinase contains a mutation that permanently inactivates it, no response is seen in cells when an extracellular signal is received. A mutation that permanently activates barley results in a response even when there is no extracellular signal. You characterize a double mutant in which hops has the inactivating mutation and barley has the activating mutation. You observe that a response is seen in the double mutants even in the absence of an extracellular signal. In the normal signaling pathway, does barley phosphorylate hops or does hops phosphorylate barley? Briefly explain your answer.
You have developed an activator of a non-receptor tyrosine kinase. In three different cell types that all contain this receptor your drug has different effects. In cell type A you see activation of gene X and gene Y; in cell type B you note activation of Gene X, but no change in the mRNA levels for Gene Y. In cell type C your drug has no effect on either Gene X or Y. Describe how could each choice (A-D) be a possibility to suit the scenario? a. Genes X & Y are controlled by two separate STATs (STAT X & STAT Y). Cell type A contains both STATs; cell type B contains STAT X only; cell type C has neither STAT. b. Genes X & Y are controlled by two separate STATs (STAT X & STAT Y) and two separate JAKs (JAK X & JAK Y). Cell type A contains both STATs and JAKs; cell type B contains both STATs but JAK X only; cell type C has both STATs but neither JAK. c. Genes X & Y are controlled by two separate STATs (STAT X & STAT Y), two separate JAKs (JAK X & JAK Y) and…
What is a signal sequence, and what is it recognized by? In what cellular process do signal sequences play a critical role?
Given the following schematic for a gene and its associated regulatory regions, answer the following questions by placing the correct letter in the provided blanks please put in the correct letter for the questions What region would provide cell type-specific expression of genes? region What site would significantly increase gene expression rates? = region What region or regions of this gene’s coding sequence are expressed as amino acids = region
Using examples, describe the signalling pathway from receptor tyrosinekinase activation to gene transcription, highlighting key phosphorylationevents and domains involved
Describe the action of the following molecular playersin signal transduction pathways: growth factors, growthfactor receptors, kinase cascades, and transcriptionfactors
Figure 9.8 HER2 is a receptor tyrosine kinase. In 30 percent of human breast cancers, HER2 is permanently activated, resulting in unregulated cell division. Lapatinib, a drug used to treat breast cancer, inhibits HER2 receptor tyrosine kinase autophosphorylation (the process by which the receptor adds phosphates onto itself), thus reducing tumor growth by 50 percent. Besides autophosphorylation, which of the following steps would be inhibited by Lapatinib? Signaling molecule binding, dimerization, and the downstream cellular response. Dimerization, and the downstream cellular response. The downstream cellular response. Phosphatase activity, dimerization, and the downsteam cellular response.
How is an extracellular signal converted to an intracellular signal in signal transduction? Give a specific example.
If some cell-surface receptors, including Notch, can rapidly signal to the nucleus by activating latent transcription regulators at the plasma membrane, why do most cell- surface receptors use long, indirect signaling cascades to influence gene transcription in the nucleus?
Fill in the gap Although signal transduction pathways are modeled mostly by ----------, there are some underlying difficulties in the modeling. Therefore, it is necessary to develop -------- to capture the details of signaling pathways by exploiting high-throughput ------------