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Recombinant constructs and transgenic fluorescent ornamental fish therefrom

a technology of transgenic ornamental fish and recombinant constructs, which is applied in the field of transgenic gene constructs with, can solve the problems of limited progress in the field of ornamental fish industry, striped pigmentation of adult zebrafish does not aid in the efficient display of various colors, etc., and achieves the highest visible fluorescence level, strong visible fluorescence, and the effect of ensuring stability of expression

Inactive Publication Date: 2010-02-25
GLOFISH LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0013]In another preferred embodiment, the fish for use with the disclosed constructs and methods is the Golden zebrafish. Zebrafish skin color is determined by pigment cells in their skin, which contain pigment granules called melanosomes. The number, size and density of the melanosomes per pigment cell influence the color of the fish skin. Golden zebrafish have diminished number, size, and density of melanosomes and hence have lighter skin when compared to the wild type zebrafish. Golden zebrafish have a mutation in slc24a5 gene, rendering the fish skin lighter or less pigmented (Lamason et al., 2005).

Problems solved by technology

However, for the ornamental fish industry the dark striped pigmentation of the adult zebrafish does not aid in the efficient display of the various colors that are currently available in the market.
All of these transgenic experiments have aimed at developing newer markers and reporters for transgenesis; however, progress in the field of ornamental fish industry has been limited.

Method used

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  • Recombinant constructs and transgenic fluorescent ornamental fish therefrom
  • Recombinant constructs and transgenic fluorescent ornamental fish therefrom
  • Recombinant constructs and transgenic fluorescent ornamental fish therefrom

Examples

Experimental program
Comparison scheme
Effect test

example 1

Design and Generation of the Construct Plasmids

[0078]The promoter of the zebrafish fast skeletal muscle myosin light chain (zMLC2) (Ju et al., 2003) and the carp β-actin enhancer / promoter sequence (Lui et al., 1990) were cloned into pBluescript II SK (−) and pUC18 respectively. Red fluorescent protein gene, DsRed2; green fluorescent protein gene, ZsGreen1 and yellow fluorescent protein gene, ZsYellow1 were amplified by PCR from pDsRed2-N1, pZsGreen1-N1 and pZsYellow1-N1 (Clontech Inc., Matz. et al., 1999) respectively and cloned into pBluescript II SK (−) zMLC2 and pUC 18-carp β-actin such that the promoter was operably linked to the fluorescent gene. Tandem SV40(A) polyA / 3′UTR sequence from pK-SV40(A)X2 plasmid were cloned 3′ to the fluorescent protein gene coding region. It is preferred to use more than one copy of the selected polyadenylation sequence, and more preferred to use a viral polyadenylation sequence, as this will increase the efficiency of the fluorescent protein gene ...

example 2

Preparation of the Construct for Delivery

[0079]The vectors pUC18-carp β-actin-DsRed2 and pUC18-carp β-actin-ZsGreen1 were restriction double digested with XbaI and AatII enzymes for three hours (FIG. 6, Step 1) and then run on 0.8% agarose gel to separate the transgenic insert cassette from the vector backbone (FIG. 6, Step 2 and 3). Transgenic insert cassette band (˜3.5 kb) which contained the promoter, the open reading frame and the 3′UTR was excised and purified using phenol:choloroform extraction.

[0080]The transgenic vectors pBluescript II SK(−)-zMLC-DsRed2-SV40x2, pBluescript II SK(−)-zMLC-ZsGreen1-SV40x2, and pBluescript II SK(−)-zMLC-ZsYellow1-SV40x2 were restriction triple digested with XhoI, XmnI and NotI enzymes for three hours and then run on 0.8% agarose gel to separate the transgenic insert cassette from the vector backbone. The transgenic insert cassette band (˜3.2 kb) which contained the promoter, the open reading frame and the 3′UTR was excised and gel purified.

example 3

Making the Transgenic Fish

[0081]The purified transgenic insert cassette which contained the promoter, the open reading frame and the 3′UTR was microinjected into the zebrafish embryos (FIG. 6, Step 4).

[0082]While only one construct was injected into Yellow zebrafish 1, to increase the chances of developing a fish with strong visible fluorescence, more than one construct was injected simultaneously in Red zebrafish 1 and Green zebrafish 1. For the purposes of this application, strong visible fluorescence means that a person with 20 / 20 vision (i.e., average vision) will be able to distinguish between the fluorescent fish in question and a non-fluorescent fish of the same species at a distance of at least 5 feet in a lighted office, with a preferred distance of at least 10 feet in a lighted office, and a more preferred distance of at least 15 feet in a lighted office, and an even more preferred distance of at least 20 feet in a lighted office, with the illumination level defined in Tab...

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Abstract

The present invention relates to the method and use of reef coral fluorescent proteins in making transgenic red, green and yellow fluorescent zebrafish. Preferably, such fluorescent zebrafish are fertile and used to establish a population of transgenic zebrafish and to provide to the ornamental fish industry for the purpose of marketing. Thus, new varieties of ornamental fish of different fluorescence colors from a novel source are developed.

Description

[0001]The present application claims the benefit of previously filed provisional application Ser. Nos. 60 / 838,006, filed Aug. 16, 2006, and 60 / 842,721, filed Sep. 7, 2006, the disclosures of which are incorporated by reference herein in their entirety.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]This invention relates to transgenic gene constructs with fish gene promoters and heterologous genes for generation of transgenic fish, particularly fluorescent transgenic fish.[0004]2. Description of Related Art[0005]Transgenic technology involves the transfer of a foreign gene into a host organism enabling the host to acquire a new and inheritable trait. The technique was first developed in mice by Gordon et al. (1980). They injected foreign DNA into fertilized eggs and found that some of the mice developed from the injected eggs retained the foreign DNA. Applying the same technique, Palmiter et al. (1982) introduced a chimeric gene containing a rat growth hormone gene u...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A01K67/027C12N15/00
CPCA01K67/0275A01K2217/05A01K2227/40A01K2267/0393A01K67/027C12N15/8509C12N2830/008G06Q99/00C07K14/43595A01K2217/052A01K2217/206
Inventor BLAKE, ALANCROCKETT, RICHARDESSNER, JEFFREYHACKETT, PERRYNASEVICIUS, AIDAS
Owner GLOFISH LLC
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