Post-transcriptional Mechanisms in Endocrine Regulation


Book Description

This book examines how post-transcriptional mechanisms control endocrine function. This includes newly identified regulatory mechanisms involved in hormone biosynthesis, control of hormone receptors and the outputs of hormone mediated signal transduction. Chapters address endocrine hormones including protein peptide/peptide, steroid, and non-steroidal hormones. The impacts of these mechanisms on disease and health are covered, providing a novel update to the scientific literature. Post-transcriptional regulatory mechanisms play an essential role in controlling dynamic gene expression. The outcome of this regulation includes control of the amount, timing, and location of protein expression. Regulation is mediated by cis-acting RNA sequences and structures and transacting RNA binding proteins and non-coding RNAs, including microRNAs. Recent advances in characterization of these regulatory factors have revealed enormous regulatory potential.













Genomics-Based Studies Identify Cis and Trans Acting Posttranscriptional Regulators


Book Description

The identity of every organism is stored in its genetic material. Each gene is transcribed into an intermediate RNA molecule, which undergoes complex processing before translation into a functional protein. RNA processing is controlled by RNA binding proteins (RBPs). Each RBP binds to and regulates the processing, stability, and translation of hundreds to thousands of RNA targets, thereby making these proteins essential for organismal development. RBPs bind to their targets by recognizing both the RNA sequence and secondary structure, which is the interaction between complementary RNA sequences within a single molecule. These interactions can be regulated by changing the chemical makeup of RNA nucleotides via covalent modification, thereby altering the secondary structure and RBP-binding of an RNA molecule. Therefore, the interplay between covalent modifications, secondary structure, and RNA-protein interactions regulates the processing and regulation of each RNA transcript. In this dissertation, I have examined these cis and trans acting post-transcriptional regulators to determine their role in RNA processing. To do this, we have applied a next generation sequencing technique to globally identify RNA-protein interactions and RNA secondary structure in the nuclei of Arabidopsis seedlings. This work has revealed a strong anti-correlation between RNA structure and protein binding. We next utilized this same technique to help identify RBPs that regulate root hair cell development. Hair cells are located on the root epidermis and are responsible for the uptake of water and nutrients from the environment. Therefore, increasing hair cell number can increase plant survival. During this work, we identified two RBPs that regulate root hair cell fate, one of which functions in the phosphate starvation response pathway. These findings reveal novel pathways involved in this developmental process. Finally, we examined the role of covalent modifications in RNA processing. By identifying modifications across the nuclear and cytoplasmic transcriptomes, we found broad populations of modifications corresponding to altered stability. These results illustrate the various regulatory roles held by covalent modifications. Together, this work has advanced the field of post-transcriptional regulation using the model plant Arabidopsis thaliana, by identifying fundamental features of RNA processing, and has raised many questions for future studies to address.










Identifying Cis-regulatory Elements and Trans-acting Factors that Activate Transcription in the Suspensor of Plant Embryos


Book Description

Seed crops, such as corn and soybean, are a major source of food for human and animal consumption. Understanding how genes are regulated in seeds is essential for the future development of genetically engineered seed crops that could significantly augment the food supply available for a rapidly growing human population. Given the importance of understanding the processes controlling seed development, it is surprising that the gene regulatory networks operating in seeds remain largely unknown. I have been using scarlet runner bean (SRB; Phaseolus coccineus), a close relative of soybean, to characterize a gene regulatory network active during early embryo development. Specifically, I have focused on gene activity in the suspensor, a specialized embryonic region involved in synthesizing and transporting nutrients to the growing embryo. To identify suspensor cis-regulatory sequences, I performed promoter dissection experiments on the SRB G564 gene, which is expressed in the suspensor early in embryo development. A 54-bp DNA fragment within the G564 upstream region is sufficient for suspensor-specific transcription in transgenic tobacco and Arabidopsis, indicating the suspensor transcriptional machinery is conserved in flowering plants. Mutagenesis of the 54- bp fragment identified five suspensor cis-regulatory elements: (i) three 10-bp motifs with the consensus 5'-GAAAAGCGAA-3', (ii) a Region 2 sequence 5'-TTG(A/G)(A/G/T)AAT-3' and (iii) a Fifth motif 5'-(A/G)AGTTA-3'. The Fifth motif sequence is a predicted MYB transcription factor binding site. A yeast one-hybrid screen identified three MYB transcription factors that bind to the 54-bp fragment and are expressed in the suspensor of Arabidopsis. Promoter deletion and mutagenesis experiments uncovered that sequences similar to these three types of suspensor motifs also activate suspensor transcription in the SRB GA 20-oxidase gene, which encodes an enzyme required for synthesis of the phytohormone gibberellic acid. The SRB G564 and GA 20-oxidase genes are activated by the same suspensor cis-regulatory elements and thus comprise a suspensor gene regulatory network, which is activated shortly after fertilization by transcriptional machinery that is conserved in the suspensors of flowering plants.