Comparison of seven housekeeping genes expression in microalgae (Chlorella vulgaris) grown under nitrogen limited condition
The study of the lipid synthesis pathway and the gene expression analysis of microalgae is crucial to understand more about the genes that play roles in lipid synthesis. The use of real-time polymerase chain reaction (PCR) in gene expression analysis is the best choice and it necessitates housekee...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Penerbit Universiti Kebangsaan Malaysia
2020
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| Online Access: | http://journalarticle.ukm.my/17233/ http://journalarticle.ukm.my/17233/1/49_04_18.pdf |
| Summary: | The study of the lipid synthesis pathway and the gene expression analysis of microalgae is crucial to understand more about
the genes that play roles in lipid synthesis. The use of real-time polymerase chain reaction (PCR) in gene expression analysis
is the best choice and it necessitates housekeeping genes (HKGs) as internal standard controls. It is essential to establish
stable reference genes for the proper normalization. This study aimed at evaluating the stability of seven HKGs of microalgae,
Chlorella vulgaris which were actin, alpha-tubulin, beta-tubulin, elongation factor, cyclophilin, 18S rRNA, and GAPDH that
were grown under nitrogen-limited condition. C. vulgaris were grown in complete F/2 media with NaNO3 concentration of
8.82 x 10-4 M for control and 2.2 x10-4 M (25%) of NaNO3 for the nitrogen-limited condition. The cultures were grown for
28 days and RNA extraction was done at intervals of 7 days. Cycle threshold (Ct) values of control and treatment were
generated from real-time PCR to evaluate the stability of HKGs. Results showed a significant stable expression of cyclophilin
(28.04 ± 1.10 for control and 29.17 ± 1.06 for treatment) and GAPDH (37.23 ± 0.30 for control and 36.44 ± 0.53 for
treatment). Meanwhile, other HKGs showed significant unstable expression. Thus, cyclophilin and GAPDH can be used as
a reference gene of C. vulgaris for lipid production. |
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