Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis

Ribosome assembly and protein translation process are regulated by ABCF1 gene. Since the function of ABCFI gene is ribosome assembly regulation, the loss of this function may cause the failure to make proteins in an organism. The purpose of this study is to clone the ABCFI gene of Rasbora sarawak...

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Main Author: Clarissa, Patrick Balinu
Format: Final Year Project Report
Language:English
English
Published: Universiti Malaysia Sarawak, (UNIMAS) 2016
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Online Access:http://ir.unimas.my/id/eprint/15461/3/Clarissa%20Patrick%20Balino%2024pgs.pdf
http://ir.unimas.my/id/eprint/15461/6/Clarissa%20Patrick%20Balino%20ft.pdf
http://ir.unimas.my/id/eprint/15461/
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Institution: Universiti Malaysia Sarawak
Language: English
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spelling my.unimas.ir.154612023-01-19T07:10:38Z http://ir.unimas.my/id/eprint/15461/ Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis Clarissa, Patrick Balinu Q Science (General) Ribosome assembly and protein translation process are regulated by ABCF1 gene. Since the function of ABCFI gene is ribosome assembly regulation, the loss of this function may cause the failure to make proteins in an organism. The purpose of this study is to clone the ABCFI gene of Rasbora sarawakensis into pGEM-T easy vector and analyse the extracted gene sequence from R. sarawakensis. Total RNA was extracted from a whole fish homogenate via Tri reagent and phenol chloroform precipitation. The cDNA generated from reverse transcription was amplified with PCR using degenerate primers targeting the conserved region of the gene. The PCR amplified amplicons of size approximately 803 bp and was inserted into pGEM-T easy vector. Transformation was performed using in-house prepared E. coli JM109 competent cell which has the efficiency of 1.57 x 104 transformants/μg. The white colonies were run in colony PCR and confirmed to have an insert. Further confirmation was conducted by performing Nod restriction digestion and the result shows two discreet bands. Afterwards, the plasmid that was obtained from plasmid miniprep was sent for sequencing and the result was corroborated by using BLAST and it shows highest similarity to gene of Sinocyclocheilus anshuiensis. Based on this study, further study of expression analysis can be conducted which can lead to the understanding of the temporal and spatial patterns of gene expression that can help assign function to genes, thus establishing R. sarawakensis as a model of study to detect eco-toxicity of Sarawakian rivers. Universiti Malaysia Sarawak, (UNIMAS) 2016 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/15461/3/Clarissa%20Patrick%20Balino%2024pgs.pdf text en http://ir.unimas.my/id/eprint/15461/6/Clarissa%20Patrick%20Balino%20ft.pdf Clarissa, Patrick Balinu (2016) Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis. [Final Year Project Report] (Unpublished)
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
English
topic Q Science (General)
spellingShingle Q Science (General)
Clarissa, Patrick Balinu
Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis
description Ribosome assembly and protein translation process are regulated by ABCF1 gene. Since the function of ABCFI gene is ribosome assembly regulation, the loss of this function may cause the failure to make proteins in an organism. The purpose of this study is to clone the ABCFI gene of Rasbora sarawakensis into pGEM-T easy vector and analyse the extracted gene sequence from R. sarawakensis. Total RNA was extracted from a whole fish homogenate via Tri reagent and phenol chloroform precipitation. The cDNA generated from reverse transcription was amplified with PCR using degenerate primers targeting the conserved region of the gene. The PCR amplified amplicons of size approximately 803 bp and was inserted into pGEM-T easy vector. Transformation was performed using in-house prepared E. coli JM109 competent cell which has the efficiency of 1.57 x 104 transformants/μg. The white colonies were run in colony PCR and confirmed to have an insert. Further confirmation was conducted by performing Nod restriction digestion and the result shows two discreet bands. Afterwards, the plasmid that was obtained from plasmid miniprep was sent for sequencing and the result was corroborated by using BLAST and it shows highest similarity to gene of Sinocyclocheilus anshuiensis. Based on this study, further study of expression analysis can be conducted which can lead to the understanding of the temporal and spatial patterns of gene expression that can help assign function to genes, thus establishing R. sarawakensis as a model of study to detect eco-toxicity of Sarawakian rivers.
format Final Year Project Report
author Clarissa, Patrick Balinu
author_facet Clarissa, Patrick Balinu
author_sort Clarissa, Patrick Balinu
title Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis
title_short Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis
title_full Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis
title_fullStr Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis
title_full_unstemmed Isolation and cloning of ABCF1 gene from Rasbora Sarawakensis
title_sort isolation and cloning of abcf1 gene from rasbora sarawakensis
publisher Universiti Malaysia Sarawak, (UNIMAS)
publishDate 2016
url http://ir.unimas.my/id/eprint/15461/3/Clarissa%20Patrick%20Balino%2024pgs.pdf
http://ir.unimas.my/id/eprint/15461/6/Clarissa%20Patrick%20Balino%20ft.pdf
http://ir.unimas.my/id/eprint/15461/
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