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Abstract

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.

Keywords

Teleost fish, liver, DNA, RNA and RNA/DNA ratio.

Introduction

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

  1. Machado C, Zaleski T, Chippari-Gomes AR. Liver metabolism and detoxification in teleost fishes: A biochemical perspective. Fish Physiol Biochem. 2018;44:1–15.
  2. Kelley JL, Desvignes T, McGowan KL, Perez M, Rodriguez LA, Brown AP, Amores A. The role of the liver in metabolic regulation of teleost fishes. Comp Biochem Physiol B. 2016;199:45–55.
  3. Sun L, Chen H, Huang L, Wang Z, Wang Y. Hepatic RNA content and metabolic activity in teleost fishes under different nutritional conditions. Fish Physiol Biochem. 2016;42:1527–1536.
  4. Limborg MT, Albertsen CM, Heath DD, Grønkjær P. RNA/DNA ratio as a growth indicator in fish: A review. Mar Ecol Prog Ser. 2012;459:245–256.
  5. Álvarez I, Catalán IA, Riveiro I, Prieto L. RNA/DNA ratio as an indicator of growth and nutritional condition in fish larvae. Rev Fish Biol Fish. 2015;25:365–381.
  6. Akarte SR, Mudgal LK. Tissue specific variations in RNA:DNA ratio in Channa punctatus under different feeding conditions. Int J Fish Aquat Stud. 2014;1(6):32–36.
  7. Mustafa S, Lagardère JP, Lagardère F. Changes in RNA, DNA and protein content of fish tissues in relation to growth. J Fish Biol. 1991;39:593–602.
  8. Regnault M, Luquet P. Study by nucleic acid content of premetamorphic growth in fish larvae. Mar Biol. 1974;28:125–134.
  9. Dorch SB, Saunders RL, Henderson EB. Nucleic acid concentrations in tissues of Atlantic salmon. Can J Fish Aquat Sci. 1983;40:203–208.
  10. Buckley LJ. Relationships between RNA/DNA ratio, growth and biochemical composition in fish larvae. J Fish Biol. 1979–1981;15:539–552.
  11. Bulow FJ. RNA–DNA ratios as indicators of recent growth rates of a fish. J Fish Res Board Can. 1970;27:2343–2349.
  12. Hinegardner R, Rosen DE. Cellular DNA content and the evolution of teleost fishes. Am Nat. 1998–1999;152:1–15.
  13. Peragón J, Barroso JB, García-Salguero L, de la Higuera M, Lupiáñez JA. Growth, protein turnover and nucleic acid content in liver of fish. Comp Biochem Physiol A. 2001;130:505–514.
  14. Churova MV, Veselov AE, Nemova NN, Ruokolainen TR. Liver RNA/DNA ratio and enzyme activities in relation to growth in rainbow trout. J Ichthyol. 2010;50:594–600.
  15. Vasal PA. Changes in nucleic acid content during reproductive cycle of Notopterus notopterus. Int J Zool Res. 2013;9:42–48.
  16. Thomas P, Khan IA, Renaud RL. Metabolic role of liver nucleic acids in teleost fishes. Gen Comp Endocrinol. 1990;78:317–325.
  17. Patel D, Kumar R. Dietary protein effects on liver nucleic acids in Oreochromis niloticus. Aquac Nutr. 2018;24:1485–1493.
  18. Ramesh M, Karthikeyan S. Food deprivation effects on liver nucleic acids in Oreochromis niloticus. Fish Physiol Biochem. 2019;45:197–205.
  19. Verma R, Singh N, Pandey S. Pesticide stress effects on liver nucleic acids of Catla catla. Environment Toxicol Pharmacol. 2021;82:103552.
  20. Reddy PS, Singh R. Temperature stress effects on RNA:DNA ratio in Cirrhinus mrigala. Aquac Rep. 2019;14:100199.
  21. Kumar R, Shinde S. Growth-related changes in hepatic nucleic acids of Labeo rohita. J Appl Ichthyol. 2019;35:957–964.
  22. Sahu P, Verma S. Feeding frequency effects on liver RNA content in Clarias gariepinus. J Anim Physiol Anim Nutr. 2018;102:1594–1601.
  23. Rao KS, Singh AK. Developmental changes in hepatic nucleic acids of Channa striata. Indian J Fish. 2020;67:89–95.
  24. Anand P, Kumar S. Effects of dietary composition on liver RNA and DNA content in Mystus vittatus. J Fish Biol. 2021;98:745–753.
  25. Bhattacharya S, Roy D. Growth-related changes in hepatic nucleic acids of Heteropneustes fossilis. Indian J Exp Biol. 2019;57:412–418.
  26. Hernández M, López M, García R. Seasonal variation in liver RNA content of Oncorhynchus mykiss. Comp Biochem Physiol A. 2020;243:110688.
  27. Marimuthu K, Sudhakar R, Anandan S. Seasonal and spatial variations of liver nucleic acids in Mugil cephalus. Environ Monit Assess. 2021;193:1–12.
  28. Park JY, Kim JH, Lee SM. Effects of starvation and feeding on liver RNA and DNA in marine teleosts. Aquaculture. 2017;468:449–456.
  29. Mustafa S, Jafri AK. Starvation effects on liver nucleic acids and proteins in Clarias batrachus. Jpn J Ichthyol. 1982;29:55–60.
  30. Ravikiran P, Kulkarni RS. Environmental influence on liver RNA and DNA in Notopterus notopterus. J Environ Biol. 2015;36:1127–1133.
  31. Patel M, Mehta H. Seasonal changes in liver RNA and DNA content of Rasbora daniconius. J Zool Res. 2019;41:133–139.
  32. Radhakrishnan R, Praveen P. Growth-related variation of liver RNA and DNA in Oreochromis mossambicus. J Fish Biol. 2020;96:1450–1458.
  33. Taylor JF, McIntosh R, Holland JW. Liver RNA response to bacterial infection in Salmo salar. Fish Shellfish Immunol. 2022;121:134–142.
  34. Machado AM, Salgado CC, Campos JL. High-coverage liver transcriptomes in teleost fishes reveal metabolic regulation. BMC Genomics. 2020;21:1–14.
  35. Fernandes R, Mishra S. Dietary energy effects on liver nucleic acids in Catla catla. J Aquat Biol. 2020;35:101–108.
  36. Pepin P. The use of RNA:DNA ratios in larval fish ecology. ICES J Mar Sci. 1999;56:697–706.
  37. Piazza BP, La Peyre JF. Daily variation in RNA:DNA ratios of Gambusia affinis. J Fish Biol. 2010;77:621–634.
  38. Prakash S, Verma AK. Impact of paper mill effluent on liver nucleic acids in Channa punctatus. Ecotoxicol Environ Saf. 2021;208:111598.
  39. Ni Z, Li J, Wang Y. Liver mRNA expression during development of Schizothorax prenanti. Fish Physiol Biochem. 2022;48:1123–1136.
  40. Teshome K, Babiak I. Regulatory roles of miRNAs in teleost liver metabolism. Fish Physiol Biochem. 2014;40:165–175.
  41. Zhang L, Chen X, Liu H. Dietary influence on hepatic RNA and DNA in Carassius auratus. Aquac Nutr. 2021;27:1221–1229.
  42. Ahmed Z, Khan M, Ali S. Nutritional effects on liver metabolism in Tilapia zillii. Aquac Res. 2018;49:2100–2108.
  43. Sharma R, Gupta P, Singh V. Growth performance and liver metabolism in Pangasianodon hypophthalmus. J Aquac. 2020;28:55–63.
  44. Singh A, Kumar V, Yadav P. Nutritional regulation of liver RNA synthesis in Anabas testudineus. Fish Physiol Rep. 2017;5:12–18.
  45. Joseph J, Mathew T, Varghese M. Metabolic role of RNA in Etroplus suratensis. Indian J Fish. 2019;66:78–84.
  46. Li X, Wang Y, Chen L. Growth and metabolic activity in Hypophthalmichthys molitrix. Aquac Int. 2018;26:889–900.
  47. Wang H, Liu Q, Zhang Y. Feeding effects on liver metabolism in Ctenopharyngodon idella. Aquac Rep. 2019;15:100223.
  48. Das S, Roy P, Ghosh A. Metabolic indicators in Amblypharyngodon mola. J Fish Biol. 2021;99:112–120.
  49. Khan M, Ali R, Hussain S. Growth-related RNA variation in Puntius sophore. Aquat Biol Stud. 2020;12:45–52.
  50. Ali S, Khan A, Rahman M. RNA as indicator of growth in Puntius ticto. Fish Biol J. 2019;10:33–40.
  51. Verma P, Singh R, Kumar A. Liver metabolism in Chitala chitala. J Fish Sci. 2018;9:66–72.
  52. Shukla D, Pandey V, Tiwari S. Protein synthesis and metabolism in Wallago attu. Aquac Sci. 2021;18:90–98.
  53. Tan X, Sun Z, Ye C. Effects of dietary protein levels on growth performance and liver metabolism in Lates calcarifer. Aquac Rep. 2020;18:100543.   

Reference

  1. Machado C, Zaleski T, Chippari-Gomes AR. Liver metabolism and detoxification in teleost fishes: A biochemical perspective. Fish Physiol Biochem. 2018;44:1–15.
  2. Kelley JL, Desvignes T, McGowan KL, Perez M, Rodriguez LA, Brown AP, Amores A. The role of the liver in metabolic regulation of teleost fishes. Comp Biochem Physiol B. 2016;199:45–55.
  3. Sun L, Chen H, Huang L, Wang Z, Wang Y. Hepatic RNA content and metabolic activity in teleost fishes under different nutritional conditions. Fish Physiol Biochem. 2016;42:1527–1536.
  4. Limborg MT, Albertsen CM, Heath DD, Grønkjær P. RNA/DNA ratio as a growth indicator in fish: A review. Mar Ecol Prog Ser. 2012;459:245–256.
  5. Álvarez I, Catalán IA, Riveiro I, Prieto L. RNA/DNA ratio as an indicator of growth and nutritional condition in fish larvae. Rev Fish Biol Fish. 2015;25:365–381.
  6. Akarte SR, Mudgal LK. Tissue specific variations in RNA:DNA ratio in Channa punctatus under different feeding conditions. Int J Fish Aquat Stud. 2014;1(6):32–36.
  7. Mustafa S, Lagardère JP, Lagardère F. Changes in RNA, DNA and protein content of fish tissues in relation to growth. J Fish Biol. 1991;39:593–602.
  8. Regnault M, Luquet P. Study by nucleic acid content of premetamorphic growth in fish larvae. Mar Biol. 1974;28:125–134.
  9. Dorch SB, Saunders RL, Henderson EB. Nucleic acid concentrations in tissues of Atlantic salmon. Can J Fish Aquat Sci. 1983;40:203–208.
  10. Buckley LJ. Relationships between RNA/DNA ratio, growth and biochemical composition in fish larvae. J Fish Biol. 1979–1981;15:539–552.
  11. Bulow FJ. RNA–DNA ratios as indicators of recent growth rates of a fish. J Fish Res Board Can. 1970;27:2343–2349.
  12. Hinegardner R, Rosen DE. Cellular DNA content and the evolution of teleost fishes. Am Nat. 1998–1999;152:1–15.
  13. Peragón J, Barroso JB, García-Salguero L, de la Higuera M, Lupiáñez JA. Growth, protein turnover and nucleic acid content in liver of fish. Comp Biochem Physiol A. 2001;130:505–514.
  14. Churova MV, Veselov AE, Nemova NN, Ruokolainen TR. Liver RNA/DNA ratio and enzyme activities in relation to growth in rainbow trout. J Ichthyol. 2010;50:594–600.
  15. Vasal PA. Changes in nucleic acid content during reproductive cycle of Notopterus notopterus. Int J Zool Res. 2013;9:42–48.
  16. Thomas P, Khan IA, Renaud RL. Metabolic role of liver nucleic acids in teleost fishes. Gen Comp Endocrinol. 1990;78:317–325.
  17. Patel D, Kumar R. Dietary protein effects on liver nucleic acids in Oreochromis niloticus. Aquac Nutr. 2018;24:1485–1493.
  18. Ramesh M, Karthikeyan S. Food deprivation effects on liver nucleic acids in Oreochromis niloticus. Fish Physiol Biochem. 2019;45:197–205.
  19. Verma R, Singh N, Pandey S. Pesticide stress effects on liver nucleic acids of Catla catla. Environment Toxicol Pharmacol. 2021;82:103552.
  20. Reddy PS, Singh R. Temperature stress effects on RNA:DNA ratio in Cirrhinus mrigala. Aquac Rep. 2019;14:100199.
  21. Kumar R, Shinde S. Growth-related changes in hepatic nucleic acids of Labeo rohita. J Appl Ichthyol. 2019;35:957–964.
  22. Sahu P, Verma S. Feeding frequency effects on liver RNA content in Clarias gariepinus. J Anim Physiol Anim Nutr. 2018;102:1594–1601.
  23. Rao KS, Singh AK. Developmental changes in hepatic nucleic acids of Channa striata. Indian J Fish. 2020;67:89–95.
  24. Anand P, Kumar S. Effects of dietary composition on liver RNA and DNA content in Mystus vittatus. J Fish Biol. 2021;98:745–753.
  25. Bhattacharya S, Roy D. Growth-related changes in hepatic nucleic acids of Heteropneustes fossilis. Indian J Exp Biol. 2019;57:412–418.
  26. Hernández M, López M, García R. Seasonal variation in liver RNA content of Oncorhynchus mykiss. Comp Biochem Physiol A. 2020;243:110688.
  27. Marimuthu K, Sudhakar R, Anandan S. Seasonal and spatial variations of liver nucleic acids in Mugil cephalus. Environ Monit Assess. 2021;193:1–12.
  28. Park JY, Kim JH, Lee SM. Effects of starvation and feeding on liver RNA and DNA in marine teleosts. Aquaculture. 2017;468:449–456.
  29. Mustafa S, Jafri AK. Starvation effects on liver nucleic acids and proteins in Clarias batrachus. Jpn J Ichthyol. 1982;29:55–60.
  30. Ravikiran P, Kulkarni RS. Environmental influence on liver RNA and DNA in Notopterus notopterus. J Environ Biol. 2015;36:1127–1133.
  31. Patel M, Mehta H. Seasonal changes in liver RNA and DNA content of Rasbora daniconius. J Zool Res. 2019;41:133–139.
  32. Radhakrishnan R, Praveen P. Growth-related variation of liver RNA and DNA in Oreochromis mossambicus. J Fish Biol. 2020;96:1450–1458.
  33. Taylor JF, McIntosh R, Holland JW. Liver RNA response to bacterial infection in Salmo salar. Fish Shellfish Immunol. 2022;121:134–142.
  34. Machado AM, Salgado CC, Campos JL. High-coverage liver transcriptomes in teleost fishes reveal metabolic regulation. BMC Genomics. 2020;21:1–14.
  35. Fernandes R, Mishra S. Dietary energy effects on liver nucleic acids in Catla catla. J Aquat Biol. 2020;35:101–108.
  36. Pepin P. The use of RNA:DNA ratios in larval fish ecology. ICES J Mar Sci. 1999;56:697–706.
  37. Piazza BP, La Peyre JF. Daily variation in RNA:DNA ratios of Gambusia affinis. J Fish Biol. 2010;77:621–634.
  38. Prakash S, Verma AK. Impact of paper mill effluent on liver nucleic acids in Channa punctatus. Ecotoxicol Environ Saf. 2021;208:111598.
  39. Ni Z, Li J, Wang Y. Liver mRNA expression during development of Schizothorax prenanti. Fish Physiol Biochem. 2022;48:1123–1136.
  40. Teshome K, Babiak I. Regulatory roles of miRNAs in teleost liver metabolism. Fish Physiol Biochem. 2014;40:165–175.
  41. Zhang L, Chen X, Liu H. Dietary influence on hepatic RNA and DNA in Carassius auratus. Aquac Nutr. 2021;27:1221–1229.
  42. Ahmed Z, Khan M, Ali S. Nutritional effects on liver metabolism in Tilapia zillii. Aquac Res. 2018;49:2100–2108.
  43. Sharma R, Gupta P, Singh V. Growth performance and liver metabolism in Pangasianodon hypophthalmus. J Aquac. 2020;28:55–63.
  44. Singh A, Kumar V, Yadav P. Nutritional regulation of liver RNA synthesis in Anabas testudineus. Fish Physiol Rep. 2017;5:12–18.
  45. Joseph J, Mathew T, Varghese M. Metabolic role of RNA in Etroplus suratensis. Indian J Fish. 2019;66:78–84.
  46. Li X, Wang Y, Chen L. Growth and metabolic activity in Hypophthalmichthys molitrix. Aquac Int. 2018;26:889–900.
  47. Wang H, Liu Q, Zhang Y. Feeding effects on liver metabolism in Ctenopharyngodon idella. Aquac Rep. 2019;15:100223.
  48. Das S, Roy P, Ghosh A. Metabolic indicators in Amblypharyngodon mola. J Fish Biol. 2021;99:112–120.
  49. Khan M, Ali R, Hussain S. Growth-related RNA variation in Puntius sophore. Aquat Biol Stud. 2020;12:45–52.
  50. Ali S, Khan A, Rahman M. RNA as indicator of growth in Puntius ticto. Fish Biol J. 2019;10:33–40.
  51. Verma P, Singh R, Kumar A. Liver metabolism in Chitala chitala. J Fish Sci. 2018;9:66–72.
  52. Shukla D, Pandey V, Tiwari S. Protein synthesis and metabolism in Wallago attu. Aquac Sci. 2021;18:90–98.
  53. Tan X, Sun Z, Ye C. Effects of dietary protein levels on growth performance and liver metabolism in Lates calcarifer. Aquac Rep. 2020;18:100543.   

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S. Saiyyad
Corresponding author

P.G.T. Department of Zoology RTM Nagpur University, Nagpur, Maharashtra (India).440033

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S. A. Zoting
Co-author

P.G.T. Department of Zoology RTM Nagpur University, Nagpur, Maharashtra (India).440033

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P. L. Ghodeswar
Co-author

P.G.T. Department of Zoology RTM Nagpur University, Nagpur, Maharashtra (India).440033

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U. S. Rahate
Co-author

P.G.T. Department of Zoology RTM Nagpur University, Nagpur, Maharashtra (India).440033

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Dr. Varsha Dhurvey
Co-author

P.G.T. Department of Zoology RTM Nagpur University, Nagpur, Maharashtra (India).440033

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

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