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A biochemical approach to determine ...

The University of Texas at Arlington.

A biochemical approach to determine the target site recognition mechanism of the R2 retrotransposable elements.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	A biochemical approach to determine the target site recognition mechanism of the R2 retrotransposable elements.
作者:	Thompson, Blaine K.
面頁冊數:	88 p.
附註:	Source: Masters Abstracts International, Volume: 49-06, page: .
附註:	Advisers: Shawn M. Christensen; Cedric Feschotte.
Contained By:	Masters Abstracts International49-06.
標題:	Biology, Molecular.
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1493790
ISBN:	9781124668505

A biochemical approach to determine the target site recognition mechanism of the R2 retrotransposable elements.
Thompson, Blaine K.

A biochemical approach to determine the target site recognition mechanism of the R2 retrotransposable elements. - 88 p.

Source: Masters Abstracts International, Volume: 49-06, page: .

Thesis (M.S.)--The University of Texas at Arlington, 2011.

Non-LTR Retrotransposons (NLRs) are selfish mobile genetic elements which parasitize the genomes of many organisms including humans. These elements transpose through an RNA intermediate and integrate directly into their genomic site using reverse transcription, a process called Target Primed Reverse Transcription (TPRT). Members of this family of transposons are abundant in the genomes of many eukaryotes including mammals, reptiles, fish, and insects. Several NLR family members such as R2 and NeSL-1 avoid causing deleterious mutations by specifically targeting repetitive genomic loci such as the 28S ribosomal DNA gene and the Spliced leader-1 exon respectively. This literature review focuses on the integration mechanism and evolution of NLRs, specifically R2.

ISBN: 9781124668505Subjects--Topical Terms:

226919
Biology, Molecular.

A biochemical approach to determine the target site recognition mechanism of the R2 retrotransposable elements.
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