Literature DB >> 25920501

Homeolog-specific targeted mutagenesis in Xenopus laevis using TALENs.

Shota Nakade1, Tetsushi Sakuma1, Yuto Sakane1, Yoshihiro Hara1, Atsushi Kurabayashi2, Keiko Kashiwagi2, Akihiko Kashiwagi2, Takashi Yamamoto3, Masanobu Obara4.   

Abstract

Transcription activator-like effector nucleases (TALENs) have previously been used for targeted genome editing in various organisms including Xenopus laevis. However, because of genomic polyploidization, X. laevis usually possess homeologous genes (homeologs) with quite similar sequences that make the analysis of gene function difficult. In the present study, we show methodological examples of targeted gene modification of X. laevis homeologs. The X. laevis cytoglobin gene (cygb) consists of two homeologs (xlcygba and xlcygbb), and molecular phylogenetic analysis suggested that they have potentially different functions. Thus, there is a need to establish a method of homeolog-specific gene disruption to clarify gene functions in detail. Here, we show successful examples of homeolog-specific and simultaneous gene disruption for xlcygba and xlcygbb. We found that selective digestion can be performed with at least three mismatches in TALEN target sites in both homeologs. This report paves the way for the functional analyses of X. laevis homeologs, even those containing nearly identical sequences.

Entities:  

Keywords:  Homeolog; TALEN; Targeted mutagenesis; Xenopus laevis

Mesh:

Substances:

Year:  2015        PMID: 25920501     DOI: 10.1007/s11626-015-9912-0

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol Anim        ISSN: 1071-2690            Impact factor:   2.416


  25 in total

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6.  Targeted mutagenesis of multiple and paralogous genes in Xenopus laevis using two pairs of transcription activator-like effector nucleases.

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10.  Microhomology-mediated end-joining-dependent integration of donor DNA in cells and animals using TALENs and CRISPR/Cas9.

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2.  Generation of a Xenopus laevis F1 albino J strain by genome editing and oocyte host-transfer.

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3.  An optimized method for cryogenic storage of Xenopus sperm to maximise the effectiveness of research using genetically altered frogs.

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