Expression of the Growth Hormone Gene during Early Development of Tiger Shovelnose Catfish (Pseudoplatystoma Fasciatum Linnaeus, 1766)

Erma P. Hayuningtyas, Abinawanto, Eni Kusrini, Agus Priyadi, Ratu Siti Aliah

Abstract

The early development stage of fish is crucial in fish farming, especially catfish species with cannibal characteristics, such as the Tiger Shovelnose Catfish (Pseudoplatystoma fasciatum Linnaeus 1766). Growth plays an essential role in fish’s life, which is influenced by the mechanism of growth hormone (GH). This study analyzed the level of growth hormone (GH) gene expression at several early developmental stages of Tiger Shovelnose Catfish. Samples were taken from an embryo, three days post hatched (dph) larvae to 60 dph juvenile. Isolation of mRNA was carried from the pituitary gland located at the head of the fish. Gene expression analysis was performed using RT-PCR method that compared GH/b-actin genes from band thickness. The results of the analysis showed the highest expression at 60 dph juvenile. The most significant increase in GH gene expression occurred from the egg to three dph larvae (P < 0.05), then decreased to 20 dph juvenile. The increased phenotypic growth was seen from the increased length and weight at 45 dph juveniles. This indicates the amount of growth hormone released at the juvenile stage of 20 dph, thus triggering rapid growth in the next stage at 45 dph juvenile. Growth hormones can act as growth biomarkers in Tiger Shovelnose Catfish. The novelty of this study was to determine the level of GH gene expression in Pseudoplatystoma fasciatum ornamental fish as the object of research. Suggestions for further research to explore genes related to growth mechanisms through transcriptomic and proteomic technologies.

 

Keywords: mRNA, biomarker, molecular biology, aquaculture, growth performance.

 

https://doi.org/10.55463/issn.1674-2974.49.7.21


Full Text:

PDF


References


KUSRINI E., PRIYADI A., and A. B. PRASETIO, Business challenge tiger Catfish (Pseudoplatystoma fasciatum) through controlled spawning technology. Media Akuakultur, 2015, 29(2): 79–83. http://dx.doi.org/10.15578/ma.10.2.2015.79-83

SCARABOTI P., GOVEZENSKY T., BOLCATTO P., and BARRIO R. A. Universal model for the skin coloration patterns of neotropical catfishes of the genus Pseudoplatystoma. Scientific Reports, 2020, 10(1): 1–12. http://dx.doi.org/10.1038/s41598-020-68700-0

ABDOLAHNEJAD Z., POURKAZEMI M., KHOSHKHOLGH M. R., and YARMOHAMMADI M. Expression of growth hormone gene during early development of Siberian sturgeon (Acipenser baerii). Molecular Biology Research Communications, 2015, 4(4): 181–188. http://dx.doi.org/10.22099/mbrc.2015.3166

SEALE A. P., PAVLOSKY K. K., CELINO-BRADY F. T., and LERNER D. T. Sex, salinity and sampling period dependent patterns of growth hormone mRNA expression in Mozambique tilapia. Aquaculture, 2020, 519: 734766. http://dx.doi.org/10.1016/j.aquaculture.2019.734766

ZHONG H., ZHANG X., XU Q., YAN J., HAN Z., ZHENG H., XIAO J., TANG Z., WANG F., LUO Y., and ZHOU Y. Nonadditive and Asymmetric Allelic Expression of Growth Hormone in Hybrid Tilapia. Frontiers in Genetics, 2019, 10: 961. http://dx.doi.org/10.3389/fgene.2019.00961

PETRO-SAKUMA C., CELINO-BRADY F. T., BREVES J. P., and SEALE A. P. Growth hormone regulates intestinal gene expression of nutrient transporters in tilapia (Oreochromis mossambicus). General and Comparative Endocrinology, 2020, 292: 113464. https://doi.org/10.1016/j.ygcen.2020.113464

RAHMEEI M., HOSSEINI SHEKARABI S. P., MEHRGAN M. S., and PAKNEJAD H. Assessment of dietary chaste tree (Vitex agnus-castus) fruit extract on growth performance, hemato-biochemical parameters, and mRNA levels of growth and appetite-related genes in goldfish (Carassius auratus). Aquaculture and Fisheries, 2022, 7(3): 296–303. http://dx.doi.org/10.1016/j.aaf.2021.01.007

SUTARJO G. A., REFKI M., ZUBAIDAH A., HANDAJANI H., and ANDRIAWAN S. Recombinant growth hormone supplemented on feed to the growth performance of barbodes binotatus. AACL Bioflux, 2020, 13(3): 1682–1688. http://www.bioflux.com.ro/docs/2020.1682-1688.pdf

PRAYOGO N. A., SIREGAR A. S., SUKARDI P., and BESSHO Y. Identification and expression of gonadotrophin hormones in Gouramy (Osphronemous gouramy, lacepède, 1801) under photoperiod manipulations. Biodiversitas, 2020, 21(4): 1365–1372. http://dx.doi.org/10.13057/biodiv/d210413

CELINO-BRADY F. T., PETRO-SAKUMA C. K., BREVES J. P., LERNER D. T., and SEALE A. P. Early-life exposure to 17β-estradiol and 4-nonylphenol impacts the growth hormone/insulin-like growth-factor system and estrogen receptors in Mozambique tilapia, Oreochromis mossambicus. Aquatic Toxicology, 2019, 217(808): 105336. http://dx.doi.org/10.1016/j.aquatox.2019.105336

FRANZ A.-C. FAASS O., KÖLLNER B., SHVED N., LINK K., CASANOVA A., WENGER M., D’COTTA H., BAROILLER J.-F., ULLRICH O., REINECKE M., and EPPLER E. Endocrine and local IGF-I in the bony fish immune system. MDPI Biology, 2016, 5(9): 1–13. http://dx.doi.org/10.3390/biology5010009

IBARRA-CASTRO L., WEBB K. A., and JOAN HOLT G. Molecular cloning, tissue distribution and ontogenetic expression of growth hormone in cobia, Rachycentron canadum. Revista de Biología Marina y Oceanografía, 2016, 51(2): 421–428. https://doi.org/10.4067/S0718-19572016000200018

TRIANTAPHYLLOPOULOS K. A., CARTAS D., and MILIOU H. Factors influencing GH and IGF-I gene expression on growth in teleost fish: how can aquaculture industry benefit? Reviews in Aquaculture, 2019, 12(3): 1637–1662. http://dx.doi.org/10.1111/raq.12402

BUWONO I. D., ISKANDAR I., and GRANDIOSA R. Growth hormone transgenesis and feed composition influence growth and protein and amino acid content in transgenic G3 mutiara catfish (Clarias gariepinus). Aquaculture International, 2021, 29(2): 431–451. http://dx.doi.org/10.1007/s10499-020-00628-8

CASTRO-RUIZ D., ANDREE K. B., BLONDEAU-BIDET E., FERNÁNDEZ-MÉNDEZ C., GARCÍA-DÁVILA C., GISBERT E., and DARIAS M. J. Isolation, identification, and gene expression analysis of the main digestive enzymes during ontogeny of the Neotropical catfish Pseudoplatystoma punctifer (Castelnau, 1855). Aquaculture, 2021, 543. http://dx.doi.org/10.1016/j.aquaculture.2021.737031

KUSRINI E., ALIMUDDIN M. Z., and SOELISTYOWATI D. T. Foreign growth hormone gene transmission and expression in F1 Transgenik Betta fish (Betta imbellis). Pakistan Journal of Biotechnology, 2018, 15(1): 1–9. https://pjbt.org/index.php/pjbt/article/view/97

SUDO R., KAWAKAMI Y., NOMURA K., TANAKA H. and KAZETO Y. Production of recombinant Japanese eel (Anguilla japonica) growth hormones and their effects on early-stage larvae. General and Comparative Endocrinology, 2022, 317: 113977. https://doi.org/10.1016/j.ygcen.2022.113977

JÖNSSON E. and BJÖRNSSON B. T. Physiological functions of growth hormone in fish with special reference to its influence on behavior. Fisheries Science, 2002, 68: 742–748. http://dx.doi.org/10.2331/fishsci.68.sup1_742

KURDIANTO A., FARIDAH N., YOSHIZAKI G., NURYATI S., and SETIAWATI M. Growth, Survival, and Body Composition of Transgenic Common Carp Cyprinus carpio 3rd Generation Expressing Tilapia Growth Hormone cDNA. HAYATI Journal of Bioscience, 2016, 23(3): 150–154. http://dx.doi.org/10.1016/j.hjb.2016.12.002

AYUNINGTYHIAS N., NASRULLAH H., SOELISTYOWATI D. T., KUSRINI E., and ALIMUDDIN A. Gene Transmission, Growth, and Exogeneous Growth Hormone Expression of G2 Transgenic Betta Fish (Betta imbellis). Jurnal Ilmiah Perikanan Dan Kelautan, 2021, 13(2): 181–189. http://dx.doi.org/10.20473/jipk.v13i2.25870

CHAN M. T. T., MUTTRAY A., SAKHRANI D., WOODWARD K., KIM J.-H., CHRISTENSEN K. A., KOOP B. F., and DEVLIN R. H. Sexually Dimorphic Growth Stimulation in a Strain of Growth Hormone Transgenic Coho Salmon (Oncorhynchus kisutch). Marine Biotechnology, 2021, 23: 140–148. https://doi.org/10.1007/s10126-020-10012-5


Refbacks

  • There are currently no refbacks.