دوره 5، شماره 5 - ( 4-1386 )                   جلد 5 شماره 5 صفحات 157-151 | برگشت به فهرست نسخه ها

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Rezaeian A, Kalantar S M, Farajnia S, Soleimani M, Baghi A, Aflatoonian A et al . Non-invasive evaluation of embryo morphological plasticity by designing of new transgenic gene cassette. IJRM 2007; 5 (5) :151-157
URL: http://ijrm.ir/article-1-94-fa.html
Non-invasive evaluation of embryo morphological plasticity by designing of new transgenic gene cassette. International Journal of Reproductive BioMedicine. 1386; 5 (5) :151-157

URL: http://ijrm.ir/article-1-94-fa.html


چکیده:   (2164 مشاهده)
Abstract Background: Determination of transgenic embryos from non transgenic embryos sibling is an important step in producing homozygous transgenic mice. These steps need by PCR or southern blotting followed extraction of DNA, but both techniques require skill and consume time. Objective: The aim of this study was simulation of high accuracy method using novel enhanced green fluorescent protein (EGFP) gene cassette to eliminate some consume time in livestock industry to assay high quality embryos and morphological plasticity. Materials and Methods: We modified pQE-Tri systemic vector with EGFP and IRES sequence to trace out coming planning of molecular farming transgene using co-injection method. Results: The combination of these sequences successfully showed the faint and normal expression of transgene in mouse pre-implantation stage embryos. The low rate of surviving green positive embryos as compare as only medium and physical treatments could be partly from the physical damage caused by microinjection and gene integration. Furthermore, application of the enhanced GFP marker facilitated subtle detection of asymmetrical division appeared in some of transgenic embryos. Conclusion: The results of current mouse simulation model imply that an efficient production and propagation of transgenic livestock can be done by co-injection of every economical gene with this novel transgene and also it can be suitable gene cassette for numerous experiments and study of protein behaviors in living cells.
نوع مطالعه: Original Article |

فهرست منابع
1. Chalfie M, Tu Y, Euskirchen G, Ward WW, Prasher DC. Green fluorescent protein as a marker for gene expression. Science 1994; 263: 802-805. [DOI:10.1126/science.8303295]
2. Reddy S, Rayburn H, Von Melchner H, Ruley HE. Fluorescence-activated sorting of totipotent embryonic stem cells expressing developmentally regulated lacZ fusion genes. Proc Natl Acad Sci USA 1992; 89: 6721-6725. [DOI:10.1073/pnas.89.15.6721]
3. Prasher DC. Using GFP to see the light. Trends Genet 1995; 11: 320-323. [DOI:10.1016/S0168-9525(00)89090-3]
4. Cubitt AB, Heim R, Adams SR, Boyd AE, Gross LA, Tsien RY. Understanding, improving and using green fluorescent proteins. Trends Biochem Sci 1995; 20: 448-455. [DOI:10.1016/S0968-0004(00)89099-4]
5. Misteli T, Spector DL. Applications of the green fluorescent protein in cell biology and biotechnology. Nat Biotechnol 1997; 15: 961-964. [DOI:10.1038/nbt1097-961]
6. Ward WW, Bokman SH. Reversible denaturation of Aequorea green-fluorescent protein: physical separation and characterization of the renatured protein. Biochemistry 1982; 21: 4535-4540. [DOI:10.1021/bi00262a003]
7. Takada T, Iida K, Awaji T, Itoh K, Takahashi R, Shibui A, et al. Selective production of transgenic mice using green fluorescent protein as a marker. Nat Biotechnol 1997; 15: 458-461. [DOI:10.1038/nbt0597-458]
8. Ikawa M, Kominami V, Yoshimura V, Tanaka V, Nishimune Y, Okabe M. A rapid and non-invasive selection of transgenic embryos before implantation using green fluorescent protein (GFP). FEBS Lett 1995; 375: 125-128. [DOI:10.1016/0014-5793(95)01162-8]
9. Rezaeian AH, Alimohammadian MH, Zainali S. Microsatellite Analysis of Mice TNF and Cypla2 Loci for Polymorphism: Detection and Evaluation of Genetic Contamination. Scand J Lab Anim Sci 2003; 30: 143-149.
10. Gianaroli L, Cristina MM, Ferraretti AP. Preimplantation genetic diagnosis in: Vayena E, Rowe PJ and Griffin PD Current Practices and Controversies in Assisted Reproduction. WHO, Geneva 2002; 223-243
11. Okabe M, Ikawa M, Kominami K, Nakanishi T, Nishimune Y. 'Green mice' as a source of ubiquitous green cells. FEBS Lett 1997 407: 313-319. [DOI:10.1016/S0014-5793(97)00313-X]
12. Heim R, Tsien RY. Improved green fluorescence. Nature 1995; 373: 663-664. [DOI:10.1038/373663b0]
13. Hadjantonakis AK, Gertsenstein M, Ikawa M, Okabe M, Nagy A. Generating green fluorescent mice by germline transmission of green fluorescent ES cells. Mech Dev 1998; 76: 79-90. [DOI:10.1016/S0925-4773(98)00093-8]
14. Huang WY, Aramburu J, Douglas PS, Izumo S. Transgenic expression of green fluorescence protein can cause dilated cardiomyopathy. Nat Med 2000; 6: 482-483. [DOI:10.1038/74914]
15. Devgan V, Rao MR, Seshagiri PB. Impact of embryonic expression of enhanced green fluorescent protein on early mouse development. Biochem Biophys Res Commun 2004; 313: 1030-1036. [DOI:10.1016/j.bbrc.2003.11.184]
16. Takada T, Iida K, Akasaka K, Yasue H, Torii R, Tsujimoto G, et al. Evaluation of heterologous insulator function with regard to Chromosomal position effect in the mouse blastocyst and fetus. Mol Reprod dev 2000; 57: 232-237. https://doi.org/10.1002/1098-2795(200011)57:3<232::AID-MRD4>3.0.CO;2-B [DOI:10.1002/1098-2795(200011)57:33.0.CO;2-B]
17. Han Z, Chung YG, Gao S, Latham KE. Maternal factors controlling blastomere fragmentation in early mouse embryos. Biol Reprod 2005; 72: 612-618. [DOI:10.1095/biolreprod.104.035444]
18. Handyside AH, Kontogianni EH, Hardy K Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature 1990; 344: 768-770. [DOI:10.1038/344768a0]
19. Cui KH, Putland RA, Seamark RF, Matthews CD. Precise sex selected births of mice following single cell embryo biopsy and Y-linked testis-specific gene analysis. Hum Reprod 1993; 8: 621-626. [DOI:10.1093/oxfordjournals.humrep.a138107]

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