LDR | | 00000nam u2200205 4500 |
001 | | 000000436869 |
005 | | 20200228153724 |
008 | | 200131s2019 ||||||||||||||||| ||eng d |
020 | |
▼a 9781085777155 |
035 | |
▼a (MiAaPQ)AAI13808414 |
040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 247004 |
082 | 0 |
▼a 574 |
100 | 1 |
▼a Khitun, Alexandra. |
245 | 10 |
▼a Chemoproteomic Approaches for Assaying Translation. |
260 | |
▼a [S.l.]:
▼b Yale University.,
▼c 2019. |
260 | 1 |
▼a Ann Arbor:
▼b ProQuest Dissertations & Theses,
▼c 2019. |
300 | |
▼a 161 p. |
500 | |
▼a Source: Dissertations Abstracts International, Volume: 81-03, Section: B. |
500 | |
▼a Advisor: Slavoff, Sarah A. |
502 | 1 |
▼a Thesis (Ph.D.)--Yale University, 2019. |
506 | |
▼a This item must not be sold to any third party vendors. |
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▼a Small open reading frames (<100 codons) are a repository of functional protein code which have been heretofore ignored due to artificial cut-offs imposed during genome annotation of virtually all organisms. In addition to encoding biologically active small proteins, small open reading frames also act as important translational regulatory elements which have shed light on the plasticity of some translation initiation steps.In eukaryotes, translation is a highly coordinated process that commences with the recognition of the 5' N7-methylguanosine cap of mRNA by protein eIF4E and proceeds through recruitment of the ribosome which scans the transcript for an AUG start codon. However, in some contexts, a subset of transcripts may evade this mechanism. During stress conditions when global translation is arrested transcripts with specialized post-transcriptional modifications or sequence motifs maintain capacity for protein synthesis. Similarly, previously thought to be non-coding regions of transcripts can produce protein through initiation at non-AUG start codons.This work describes a set of proteomic experiments that aim to detect and quantify regulated translation events. Chapter 1 introduces the subject of stress-regulated translation in detail, focusing on translation from small open reading frames in both prokaryotes and eukaryotes. Chapter 2 describes the discovery of bacterial stress-regulated small proteins using a semi-quantitative proteomic approach. Chapter 3 gives an example of a small protein encoded on a long non-coding RNA that mediates mucosal immunity in mice, and is conserved in humans. Chapter 4 outlines the discovery of a dual-coding transcript that co-encodes a ribosomal protein and a protein of unknown function. Chapter 5 introduces a chemical labeling strategy that uniquely facilitates detection of non-annotated proteoforms in human cells. Chapter 6 focuses specifically on stress-regulated translation in eukaryotes, and the detection of a stress-induced eIF4E regulon, Sec28, in yeast. |
590 | |
▼a School code: 0265. |
650 | 4 |
▼a Chemistry. |
650 | 4 |
▼a Biology. |
690 | |
▼a 0485 |
690 | |
▼a 0306 |
710 | 20 |
▼a Yale University.
▼b Chemistry. |
773 | 0 |
▼t Dissertations Abstracts International
▼g 81-03B. |
773 | |
▼t Dissertation Abstract International |
790 | |
▼a 0265 |
791 | |
▼a Ph.D. |
792 | |
▼a 2019 |
793 | |
▼a English |
856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T15490541
▼n KERIS
▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다. |
980 | |
▼a 202002
▼f 2020 |
990 | |
▼a ***1816162 |
991 | |
▼a E-BOOK |