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X-WR-CALNAME;VALUE=TEXT:Ava Mainieri Thesis Defense (Haig Lab)
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SUMMARY:Ava Mainieri Thesis Defense (Haig Lab)
DESCRIPTION:<p>	<strong><!--break-->Title:</strong> The Sins of Our Kin: From Genomic Imprinting to Ancient Signaling Systems</p><p>	<strong>Abstract: </strong>The bond between parents and their offspring is often regarded as something loving and supportive. But, this bond is more of a battle. Genomic imprinting is the result of the evolutionary struggle between mothers and fathers for reproductive success. The first part of the thesis describes the 3’- untranslated region (3’-UTR) of the insulin-like growth factor type 1 receptor (IGF1R) as an ancient long noncoding RNA. The 3’-UTR of the mouse <em>Igf1r</em> <span style="serif">mRNA is targeted by miR-675-3p derived from the imprinted </span><em>H19</em> <span style="serif">long noncoding RNA. We undertook a comparative analysis of vertebrate </span><em>IGF1R</em> <span style="serif">3’-UTRs to determine the evolutionary history of miR-675 target sequences and to identify conserved features that are likely to be involved in post-transcriptional regulation of IGF1R translation. The conserved structures we identify emphasize the central importance of IGF signaling pathways in the mediation of intragenomic conflicts over embryonic growth. </span></p><p>	The second part is aimed at investigating the <em>Retrotransposon Gag-like 1 (RTL1)</em> <span style="serif">and the molecular evolution of self-targeting imprinted microRNAs. Transcription of the sense strand of the </span><em>RTL1</em> <span style="serif">gene produces a protein-coding mRNA that is targeted for degradation by microRNAs transcribed from the antisense strand of the protein-coding sequence. The sense and antisense transcripts are oppositely imprinted. We present an evolutionary model for the establishment of a new self- targeting microRNA derived from within a tandem repeat that inhibits production of RTL1 protein when maternally-derived in heterozygotes but not when paternally-derived. </span></p><p>	Lastly, oxytocin has commonly been viewed as a molecule that can melt away malevolence and increase bonding. Its effects, however, are involved in the pro- cess of smooth muscle contraction. Oxytocin is a member of a nonapeptide family constituting an evolutionarily conserved signaling system found in vertebrates and invertebrates. We postulate that there is an evolutionary connection among the vari-ous functions attributed to these peptides. We believe that the acute anorexic effects of oxytocin, and its orthologs, released during egg-laying inhibits the consumption of a female’s own eggs and that the first evolutionary use of oxytocin peptides in social bonding was in the promotion of nurturing feelings towards clutches of fertilized eggs.</p><p>	<strong>Committee:</strong> David Haig (Advisor), John Wakeley</p>
LOCATION:NOT PUBLIC: ONLINE ONLY
STATUS:CONFIRMED
DTSTART:20200324T140000Z
DTEND:20200324T140000Z
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