P.G.T. Department of Zoology RTM Nagpur University, Nagpur, Maharashtra (India).440033
The liver is metabolic organ in teleost fishes and plays an important role in biochemical and physiological process. DNA and RNA, plays a crucial role in regulating growth, metabolic activity and protein synthesis in teleost fishes. Hepatic RNA content is highly responsive to dietary, developmental and environmental factors, while DNA levels remain relatively stable, serving as a genetic baseline. RNA/DNA ratios provide valuable insights into the liver’s metabolic status, growth potential and physiological condition. Present study focuses on biochemical studies on DNA and RNA in liver tissue of teleost. Studies indicate that variations in nucleic acid content reflect nutritional, environmental, and seasonal influences, making liver DNA and RNA reliable indicators of fish health and adaptive metabolic responses. Biochemical studies important for understanding enhances knowledge of liver physiology and supports effective monitoring of metabolic and growth-related processes in teleost’s.
Teleost fishes, comprising over 30,000 species, represent the largest and most ecologically diverse vertebrate group, inhabiting marine, freshwater and estuarine environments [1-2]. Their evolutionary success stems from remarkable physiological and behavioural adaptability. Among their organs, the liver is central to metabolic homeostasis, managing nutrient storage, detoxification and the regulation of carbohydrate, lipid and protein metabolism[1-2]. Accordingly, its biochemical composition especially nucleic acid content provides a reliable indicator of cellular activity and overall metabolic status DNA and RNA are the principal nucleic acids that govern genetic regulation and protein synthesis. In teleost fishes, hepatic RNA levels vary in response to feeding regimes, environmental changes and metabolic demands, while DNA content generally remains stable within cells[3-4]. As a result, the RNA/DNA ratio has been widely used as a reliable indicator of growth rate, metabolic efficiency and the capacity for protein synthesis [5-6]. RNA and DNA are essential nucleic acids present in all cells, including the liver of teleost fishes. DNA provides a stable measure of cell number and biomass, while RNA is directly involved in protein synthesis and cellular activity. Measuring RNA and DNA levels in liver tissue allows researchers to assess the molecular composition and basic biochemical status of fish cells [7-8-9]. Biochemical analyses often require cell quantity or cellularity as a reference parameter. Cellularity can be expressed in terms of cell number, cell volume, or cellular nucleic acid content and the RNA:DNA ratio is a measure of the balance between these two essential cellular components [10-11]. The accuracy of cellular nucleic acid content estimation directly affects the precision of the estimation of cellular parameters. Reliable estimation of RNA and DNA depends on the efficiency and accuracy of isolation and quantification methods.
The liver, being a central metabolism, detoxification and nutrient processing organ, is a most important target for organ-specific nucleic acid analysis. Although several studies have quantified both RNA and DNA in fish liver, these are quite limited. For example, [12] measured nuclear DNA content in a number of teleost species, but did not quantify RNA.Measuring nucleic acid content was previously used to evaluate tissue growth characteristics and protein synthesis in cultured and wild fish, including herring, Clupea harengus and mackerel, Scomber scombrus has been identified as suitable for studying the relationship between nucleic acid contents and protein and nucleotide accumulation [13]. The same has been shown for evaluating the relationship between DNA/RNA content and nucleotide composition with lipid content in the studies on herring [13].
In rainbow trout (Parasalmo mykiss), liver RNA/DNA ratios and activities of citrate synthase, cytochrome C oxidase, and lactate dehydrogenase were measured over a period of several months. It was found that RNA/DNA ratios could serve as an index of tissue growth and biomass production. The activities of these three enzymes were highly correlated with RNA/DNA ratio and this could be a result of the same stimulatory pool mechanism for the synthesis of the enzymes and structural proteins.[14] The level of nucleic acid in an organism is one of the central parameters in the assessment of various physiological conditions such as cell proliferation, biomass buildup and energy requirement. DNA and RNA content in different tissues of Notopterus notopterus was analyzed during the reproductive cycle to extrapolate the variation in nucleic acid levels in the liver during different reproductive phases of the fish. The results of the analysis indicate that nucleic acid levels vary with tissue and phase of reproduction. The findings reveal the dynamic character of nucleic acids and provide insight into nucleic acid turnover relative to the phases of the reproductive cycle and the metabolism of the specific organ.
Tissue specific variations in the RNA:DNA ratio in Channa punctatus under different feeding conditions. They found that liver exhibited distinct RNA:DNA ratios depending on nutritional status, demonstrating that the RNA:DNA ratio is a useful biochemical indicator for assessing tissue-specific metabolic activity and energy allocation in fish[6]. DNA and RNA are crucial biomolecules involved in the structure and functionality of all living cells, including those found in teleost fishes[16]. The liver is particularly metabolically active, carrying out vital functions such as nutrient processing, enzyme production and detoxification. Because of its significant metabolic activity, the liver contains considerable amounts of nucleic acids, which makes it an excellent organ for examining DNA and RNA as indicators of cellular function, metabolic activity and growth potential of tissues .[17]
DNA
From the reviewed studies, liver DNA content in fish remains relatively constant under different dietary, environmental, seasonal and physiological conditions. In Oreochromis niloticus, dietary protein variation and starvation did not significantly alter in liver DNA levels [18]. Similarly, pesticide exposure in Catla catla [19] and temperature stress in Cirrhinus mrigala [20] showed stable DNA content despite metabolic disturbances. Growth and feeding studies in Labeo rohita [21], Clarias gariepinus [22], Channa striata [23], Mystus vittatus [24] and Heteropneustes fossilis [25] consistently reported minimal variation in liver DNA levels. Even with seasonal variations in Oncorhynchus mykiss [26] and pollution stress in Mugil cephalus [27], DNA was relatively stable. These results suggested that liver DNA is a mirror of tissue cellularity and a constant reference parameter in biochemical studies.
RNA
Liver RNA content fluctuates notably as a response to the nutritional state, environmental stress, growth, and physiological conditions, unlike DNA. Oreochromis niloticus liver RNA levels increased due to higher dietary protein , while starvation led to a reduction in Oreochromis niloticus [17] , while starvation reduced RNA in RNA is known to be influenced differentially by environmental stress, growth, seasons, habitat, and temperature. Tissue depletion of RNA was observed under pesticides in Oplegnathus fasciatus and Paralichthys olivaceus [28] as well as in Clarias batrachus[29]. Pesticide exposure in Catla catla [19] and elevated temperature in Cirrhinus mrigala [20] led to decreased RNA levels, demonstrating its sensitivity to environmental stress. Seasonal and habitat-related variations in RNA were observed in Notopterus notopterus [30], Mugil cephalus [27], and Rasbora daniconius [31]. Growth-related increases in RNA were reported in Oreochromis mossambicus [32], Infection studies in Salmo salar [33] further demonstrated elevated RNA associated with immune activation. Overall, RNA is identified as a sensitive biochemical marker of metabolic activity and growth.
BIOCHEMISTRY IN LIVER
The liver is the primary organ for the regulation of physiological status and as such is very demanding in fuel and biochemical substrates for the synthesis of proteins and other molecules. The liver structure is very dynamic and heterogeneous because it changes metabolism very quickly in response to hormonal regulation (insulin and glucagon), to responses to endogenous compounds (interferons and nucleotides), and to the metabolites of amino acids (ammonia, urea and methylamines). In addition to oxidizing fatty acids to form ketone bodies, vitellogenin and other yolk proteins they are essential for egg production are also synthesized in the liver.[34] found that 1% of the chicken liver genes respond to fasting within 72 hours regardless of fasting status, approximately 8% of the genes in the liver change their expression periodically with 90 minutes of a 12- Mole/12-return light cycle. These are just a few of the responses of the liver of this organ and its relationship of metabolism in poultry.Advanced molecular studies, including transcriptomic analyses [34], further confirm that liver nucleic acids reflect metabolic regulation and adaptive responses. Collectively, the review supports the use of liver DNA as a stable cellular indicator and liver RNA as a dynamic marker of metabolic and physiological condition in fish.
Table 1: Review of DNA and RNA in different fish species
|
Model Organism |
RNA Level |
DNA Level |
Key Inference |
Reference |
|
Oreochromis niloticus |
Increase |
Increase |
Higher dietary protein enhances liver metabolism and growth activity |
Patel et al., 2018 |
|
Catla catla |
Increase |
Decrease |
Pesticide exposure reduces protein synthesis in liver |
Verma et al., 2021 |
|
Cirrhinus mrigala |
Increase |
Decrease |
Elevated temperature causes metabolic stress in liver |
Reddy et al., 2019 |
|
Labeo rohita |
Increase |
Increase |
Growth stages associated with enhanced protein synthesis |
Kumar et al., 2019 |
|
Oplegnathus fasciatus |
Increase |
Decrease |
Starvation reduces metabolic activity |
Park et al., 2017 |
|
Paralichthys olivaceus |
Increase |
Decrease |
Nutritional stress decreases RNA synthesis |
Park et al., 2017 |
|
Gadus morhua |
Increase |
Increase |
Higher RNA reflects improved growth condition |
Pepin et al., 1999 |
|
Salmo salar |
Increase |
Increase |
Immune response associated with increased RNA synthesis |
Taylor et al., 2022 |
|
Gambusia affinis |
Increase |
Increase |
Feeding increases liver metabolic activity |
Piazza et al., 2010 |
|
Clarias batrachus |
Increase |
Decrease |
Fasting decreases RNA indicating nutritional stress |
Mustafa et al., 1982 |
|
Notopterus notopterus |
Increase |
Increase |
Environmental variation affects metabolic activity |
Ravikiran et al., 2015 |
|
Channa punctatus |
Decrease |
Decrease |
Effluent pollution damages liver metabolic processes |
Prakash et al., 2021 |
|
Mugil cephalus |
Decrease |
Decrease |
Polluted environment reduces nucleic acid levels |
Marimuthu et al., 2021 |
|
Danio rerio |
Increase |
Increase |
Liver metabolism linked with nucleic acid synthesis |
Machado et al., 2020 |
|
Cyprinus carpio |
Increase |
Increase |
RNA involved in metabolic regulation |
Teshome et al., 2014 |
|
Oreochromis niloticus |
Increase |
Decrease |
Starvation decreases metabolic activity in liver |
Ramesh et al., 2019 |
|
Schizothorax prenanti |
Increase |
Increase |
Development increases metabolic activity |
Ni et al., 2022 |
|
Salmo trutta |
Increase |
Increase |
RNA increase linked with immune response |
Taylor et al., 2022 |
|
Oreochromis mossambicus |
Increase |
Increase |
Growth stages show increased metabolic activity |
Radhakrishnan et al., 2020 |
|
Carassius auratus |
Increase |
Increase |
High protein diet increases RNA synthesis |
Zhang et al., 2021 |
|
Oncorhynchus mykiss |
Increase |
Increase |
Seasonal feeding increases metabolic activity |
Hernandez et al., 2020 |
|
Labeo rohita |
Increase |
Increase |
Growth related increase in RNA synthesis |
Kumar et al., 2019 |
|
Catla catla |
Increase |
Increase |
High energy diet stimulates liver metabolism |
Fernandes et al., 2020 |
|
Clarias gariepinus |
Increase |
Increase |
Feeding frequency increases metabolic activity |
Sahu et al., 2018 |
|
Rasbora daniconius |
Increase |
Increase |
Seasonal variation affects liver metabolism |
Patel et al., 2019 |
|
Channa striata |
Increase |
Increase |
Maturity associated with enhanced biosynthetic activity |
Rao et al., 2020 |
|
Mystus vittatus |
Increase |
Increase |
Protein rich diet increases metabolic activity |
Anand et al., 2021 |
|
Heteropneustes fossilis |
Increase |
Increase |
Growth stages increase RNA synthesis |
Bhattacharya et al., 2019 |
|
Tilapia zillii |
Increase |
Increase |
Nutritional improvement enhances liver metabolism |
Ahmed et al., 2018 |
|
Pangasianodon hypophthalmus |
Increase |
Increase |
Growth associated with increased protein synthesis |
Sharma et al., 2020 |
|
Anabas testudineus |
Increase |
Increase |
Improved nutrition increases RNA synthesis |
Singh et al., 2017 |
|
Etroplus suratensis |
Increase |
Increase |
RNA indicates active metabolic processes |
Joseph et al., 2019 |
|
Hypophthalmichthys molitrix |
Increase |
Increase |
RNA linked with growth and metabolism |
Li et al., 2018 |
|
Ctenopharyngodon idella |
Increase |
Increase |
Feeding increases biosynthetic activity |
Wang et al., 2019 |
|
Amblypharyngodon mola |
Increase |
Increase |
RNA reflects metabolic health |
Das et al., 2021 |
|
Puntius sophore |
Increase |
Increase |
Growth increases metabolic activity |
Khan et al., 2020 |
|
Puntius ticto |
Increase |
Increase |
RNA increase associated with growth |
Ali et al., 2019 |
|
Chitala chitala |
Increase |
Increase |
Active metabolism reflected in RNA levels |
Verma et al., 2018 |
|
Wallago attu |
Increase |
Increase |
Feeding increases protein synthesis |
Shukla et al., 2021 |
|
Lates calcarifer |
Increase |
Increase |
RNA synthesis associated with growth activity |
Tan et al., 2020 |
CONCLUSION
The hepatic DNA and RNA content, along with the resulting RNA/DNA ratio, are established as critical and sensitive biochemical biomarkers for assessing the metabolic health and growth potential of teleost fishes. The liver, a central metabolic hub, reflects physiological state through its nucleic acid composition. While DNA provides a stable reference for cell quantity, RNA dynamically indicates the capacity for protein synthesis and metabolic intensity, which is highly responsive to nutritional status, environmental stressors and seasonal changes. Thus, monitoring liver nucleic acids provides a reliable approach for assessing the physiological and growth condition of teleost’s.
ACKNOWLEDGMENT
I would like to express our special thanks to prof. Mrs. V.T. Dhurvey, Head of Department of Zoology, RTM Nagpur University for providing all facilities required for this work.
A very special thanks to Ms. Falguni Aylanwar and Ms. Anjali Taru for providing their constant valuable guidance and precious time throughout the project.
REFERENCES
S. A. Zoting, S. Saiyyad, P. L. Ghodeswar, U. S. Rahate, Dr. Varsha Dhurvey, Biochemical Study of DNA and RNA in Liver of Teleost: A Review, Int. J. of Pharm. Sci., 2026, Vol 4, Issue 5, 2471-2478. https://doi.org/10.5281/zenodo.20126134
10.5281/zenodo.20126134