Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats

• AIM: To investigate the stability of the seven housekeeping genes: beta-actin (ActB), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), 18s ribosomal unit 5 (18s), cyclophilin A (CycA), hypoxanthine-guanine phosphoribosyl transferase (HPRT), ribosomal protein large P0 (36B4) and terminal uridylyl...

Full description

Bibliographic Details
Published in:International Journal of Ophthalmology
Main Author: Sadikan M.Z.; Nasir N.A.A.; Ibahim M.J.; Iezhitsa I.; Agarwal R.
Format: Article
Language:English
Published: International Journal of Ophthalmology (c/o Editorial Office) 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85191541129&doi=10.18240%2fijo.2024.05.02&partnerID=40&md5=cf447aa5e9ee7a9b204163a6646794e3
id 2-s2.0-85191541129
spelling 2-s2.0-85191541129
Sadikan M.Z.; Nasir N.A.A.; Ibahim M.J.; Iezhitsa I.; Agarwal R.
Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
2024
International Journal of Ophthalmology
17
5
10.18240/ijo.2024.05.02
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85191541129&doi=10.18240%2fijo.2024.05.02&partnerID=40&md5=cf447aa5e9ee7a9b204163a6646794e3
• AIM: To investigate the stability of the seven housekeeping genes: beta-actin (ActB), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), 18s ribosomal unit 5 (18s), cyclophilin A (CycA), hypoxanthine-guanine phosphoribosyl transferase (HPRT), ribosomal protein large P0 (36B4) and terminal uridylyl transferase 1 (U6) in the diabetic retinal tissue of rat model. • METHODS: The expression of these seven genes in rat retinal tissues was determined using real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) in two groups; normal control rats and streptozotocin-induced diabetic rats. The stability analysis of gene expression was investigated using geNorm, NormFinder, BestKeeper, and comparative delta-Ct (ΔCt) algorithms. • RESULTS: The 36B4 gene was stably expressed in the retinal tissues of normal control animals; however, it was less stable in diabetic retinas. The 18s gene was expressed consistently in both normal control and diabetic rats’ retinal tissue. That this gene was the best reference for data normalisation in RT-qPCR studies that used the retinal tissue of streptozotocin-induced diabetic rats. Furthermore, there was no ideal gene stably expressed for use in all experimental settings. • CONCLUSION: Identifying relevant genes is a need for achieving RT-qPCR validity and reliability and must be appropriately achieved based on a specific experimental setting. © 2024 International Journal of Ophthalmology (c/o Editorial Office). All rights reserved.
International Journal of Ophthalmology (c/o Editorial Office)
22223959
English
Article
All Open Access; Gold Open Access
author Sadikan M.Z.; Nasir N.A.A.; Ibahim M.J.; Iezhitsa I.; Agarwal R.
spellingShingle Sadikan M.Z.; Nasir N.A.A.; Ibahim M.J.; Iezhitsa I.; Agarwal R.
Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
author_facet Sadikan M.Z.; Nasir N.A.A.; Ibahim M.J.; Iezhitsa I.; Agarwal R.
author_sort Sadikan M.Z.; Nasir N.A.A.; Ibahim M.J.; Iezhitsa I.; Agarwal R.
title Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
title_short Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
title_full Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
title_fullStr Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
title_full_unstemmed Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
title_sort Identifying the stability of housekeeping genes to be used for the quantitative real-time PCR normalization in retinal tissue of streptozotocin-induced diabetic rats
publishDate 2024
container_title International Journal of Ophthalmology
container_volume 17
container_issue 5
doi_str_mv 10.18240/ijo.2024.05.02
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85191541129&doi=10.18240%2fijo.2024.05.02&partnerID=40&md5=cf447aa5e9ee7a9b204163a6646794e3
description • AIM: To investigate the stability of the seven housekeeping genes: beta-actin (ActB), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), 18s ribosomal unit 5 (18s), cyclophilin A (CycA), hypoxanthine-guanine phosphoribosyl transferase (HPRT), ribosomal protein large P0 (36B4) and terminal uridylyl transferase 1 (U6) in the diabetic retinal tissue of rat model. • METHODS: The expression of these seven genes in rat retinal tissues was determined using real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) in two groups; normal control rats and streptozotocin-induced diabetic rats. The stability analysis of gene expression was investigated using geNorm, NormFinder, BestKeeper, and comparative delta-Ct (ΔCt) algorithms. • RESULTS: The 36B4 gene was stably expressed in the retinal tissues of normal control animals; however, it was less stable in diabetic retinas. The 18s gene was expressed consistently in both normal control and diabetic rats’ retinal tissue. That this gene was the best reference for data normalisation in RT-qPCR studies that used the retinal tissue of streptozotocin-induced diabetic rats. Furthermore, there was no ideal gene stably expressed for use in all experimental settings. • CONCLUSION: Identifying relevant genes is a need for achieving RT-qPCR validity and reliability and must be appropriately achieved based on a specific experimental setting. © 2024 International Journal of Ophthalmology (c/o Editorial Office). All rights reserved.
publisher International Journal of Ophthalmology (c/o Editorial Office)
issn 22223959
language English
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
_version_ 1809678151712768000