Genetics: Analysis and Principles
Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 17, Problem 2EQ
Summary Introduction

To review:

The introduction of pre-miRNA (precursor micro Ribonucleic acid) or pre-siRNA (precursor small interfering ribonucleic acid) that cause the degradation of mex-3 RNA in Caenorhabditiselegans

Introduction:

Pre-miRNAs or pre-siRNAs are extensively used up in the process of silencing of mRNAs (messenger RNA). The pre-miRNAs undergo processing by DROSHA and DGCR8 proteins and form hairpin loop structure and the ends are cleaved by exoportin. These are directly released from the nucleus. The siRNAs and miRNAs are recognized by DICER and cleaved into dsRNA (double-stranded ribonucleic acid) and associate with other proteins to form RISC (RNA induced silencing complex) that further silences the mRNAs due to the complementary binding.

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What would be a possible result if a miRNA that perfectly complemented E3 ligase was successfully processed in the cell?
You are a research scientist studying miRNA processing. You currently know everything about the pathway except for one detail: whether Dicer resides in the nucleus or in the cytoplasm. You have an experiment setup where you have a miRNA that completely complements the GFP (green fluorescent protein) gene in a model yeast cell. You plan to mutate Exportin 5 and make it dysfunctional, then you will inject synthetic pre-miRNA either in its double strand form or its hairpin single strand form into the cell. Should you inject the synthetic pre-miRNA into the nucleus or the cytoplasm? a) b) If you inject hairpin single stranded pre-miRNA into the appropriate location in the cell, what color do you expect the yeast to be if Dicer is in the nucleus? What color would the yeast be if Dicer is in the cytoplasm? Briefly explain your reasoning.
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Genetics: Analysis and Principles

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