Insights into Evolutionary Relationships of Proboscis Monkeys Using In Silico Mitochondrial DNA Analysis

Authors

  • Rani Sasmita Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Lambung Mangkurat, Ahmad Yani Street Km. 36, Banjarbaru, South Kalimantan 70714, Indonesia
  • Badruzsaufari Badruzsaufari Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Lambung Mangkurat, Ahmad Yani Street Km. 36, Banjarbaru, South Kalimantan 70714, Indonesia
  • Intan Widya Pangestika Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Lambung Mangkurat, Ahmad Yani Street Km. 36, Banjarbaru, South Kalimantan 70714, Indonesia

DOI:

https://doi.org/10.36312/biocaster.v6i2.688

Keywords:

Colobinae, Genetic Distance, Mitochondrial DNA, Nasalis larvatus, Phylogenetics

Abstract

This study investigates the evolutionary position of the proboscis monkey (Nasalis larvatus) within the Colobinae subfamily using in silico phylogenetic analysis of three mitochondrial protein-coding genes (COI, COII, and COIII). Seventy sequences retrieved from GenBank were aligned and analyzed using the Maximum Likelihood method with 1,000 bootstrap replicates. All genes exhibited conserved lengths and strong AT bias (59,21-60,68%), reflecting typical mitochondrial genome characteristics shaped by asymmetric replication and purifying selection. Genetic distance analyses revealed high intraspecific consistency in Nasalis larvatus, while demonstrating marker dependent variation in phylogenetic resolution. COII and COIII provided clearer intergeneric separation compared to the more conserved COI marker. Phylogenetic reconstruction showed topological variation among markers, however, a consistent evolutionary signal emerged, with Nasalis larvatus clustering robustly with Simias concolor across all gene trees. This pattern supports the monophyly of the odd nosed monkey clade and aligns with genome scale phylogenomic evidence. Overall, this study highlights the limitations of single gene analyses and emphasizes the importance of multi marker or genome scale approaches for resolving complex evolutionary relationships. These findings provide foundational insights into the evolutionary history of Nasalis larvatus and reinforce the relevance of mitochondrial markers in primate conservation genetics.

Downloads

Download data is not yet available.

References

Arenson, J. L. (2024). Morphological and Molecular Systematics of the Extant Colobinae Blyth, 1863 (Primates: Cercopithecidae). Zoological Journal of the Linnean Society, 202(4), 1-38. https://doi.org/10.1093/zoolinnean/zlae152

Baleva, M. V., Chicherin, I., Piunova, U., Zgoda, V., Patrushev, M. V., Levitskii, S., & Kamenski, P. (2022). Pentatricopeptide Protein PTCD2 Regulates COIII Translation in Mitochondria of the HeLa Cell Line. International Journal of Molecular Sciences, 23(22), 1-12. https://doi.org/10.3390/ijms232214241

Bernard, H., Abram, N. K., Kuriting, J. B., & Matsuda, I. (2025). Population and Habitat of Proboscis Monkeys (Nasalis larvatus) in Northwest Sabah, Borneo, Malaysia. International Journal of Primatology, 47(1), 81–111. https://doi.org/10.1007/s10764-025-00511-4

Bi, X., Zhou, L., Zhang, J.-J., Feng, S., Hu, M., Cooper, D. N., Lin, J., Li, J., Wu, D.-D., & Zhang, G. (2023). Lineage-Specific Accelerated Sequences Underlying Primate Evolution. Science Advances, 9(22), 1-12. https://doi.org/10.1126/sciadv.adc9507

Chakraborty, S., Basumatary, P., Nath, D., Paul, S., & Uddin, A. (2022). Compositional Features and Pattern of Codon Usage for Mitochondrial CO Genes Among Reptiles. Mitochondrion, 62(1), 111–121. https://doi.org/10.1016/j.mito.2021.11.004

Doyle, E. D., Prates, I., Sampaio, I., Koiffmann, C., Silva, W. A., Carnaval, A. C., & Harris, E. E. (2021). Molecular phylogenetic inference of the Howler Monkey Radiation (Primates: Alouatta). Primates, 62(1), 177–188. https://doi.org/10.1007/s10329-020-00854-x

Finnegan, N., Lima, M. G. M., & Lynch, J. W. (2025). Mitochondrial DNA for Phylogeny Building: Assessing Individual and Grouped mtGenes as Proxies for the mtGenome in Platyrrhines. American Journal of Primatology, 87(3), 1-18. https://doi.org/10.1002/ajp.70017

Gomes-Dos-Santos, A., Vilas-Arrondo, N., Machado, A. M., Román-Marcote, E., Del Río Iglesias, J. L., Baldó, F., Pérez, M., Fonseca, M. M., Castro, L. F. C., & Froufe, E. (2023). Mitochondrial Replication’s Role in Vertebrate mtDNA Strand Asymmetry. Open Biology, 13(12), 1-11. https://doi.org/10.1098/rsob.230181

Kuang, Z., Cook, A., Ren, J., Deng, W., Cao, Y., & Cai, H. (2023). A Flat-Lying Transitional Free Gas to Gas Hydrate System in a Sand Layer in the Qiongdongnan Basin of the South China Sea. Geophysical Research Letters, 50(24), 1-10. https://doi.org/10.1029/2023GL105744

Kumar, S., Stecher, G., Suleski, M., Sanderford, M., Sharma, S., & Tamura, K. (2024). MEGA12: Molecular Evolutionary Genetic Analysis Version 12 for Adaptive and Green Computing. Molecular Biology and Evolution, 41(12), 1-9. https://doi.org/10.1093/molbev/msae263

Licuanan, A. M., & Matias, A. M. A. (2022). In Silico Evaluation of the Taxonomic Resolution and Coverage of the COI Region and Alternative Barcode Markers for Echinoderms. Philippine Journal of Science, 151(3), 955–968. https://doi.org/10.56899/151.03.14

Liu, R., Amato, K., Hou, R., Gomez, A., Dunn, D. W., Zhang, J., Garber, P. A., Chapman, C. A., Righini, N., He, G., Fang, G., Li, Y., Li, B., & Guo, S. (2022). Specialized Digestive Adaptations within the Hindgut of a Colobine Monkey. Innovation, 3(2), 1-6. https://doi.org/10.1016/j.xinn.2022.100207

Main, D. C., Taft, J. M., Geneva, A. J., van Vuuren, B. J., & Tolley, K. A. (2024). The Efficacy of Single Mitochondrial Genes at Reconciling the Complete Mitogenome Phylogeny - A Case Study on Dwarf Chameleons. PeerJ, 12(4), 1–23. https://doi.org/10.7717/peerj.17076

McDonald, M. M., Cunneyworth, P. M. K., Anderson, A. G., & Wroblewski, E. (2022). Mitochondrial Genetic Diversity and Divergence Dating of Angolan Colobus Monkeys (Colobus angolensis) in the Eastern Forests of Kenya and Tanzania: Implications for Subspeciation and Reconstructing Historical Biogeography. American Journal of Primatology, 84(7), 1-20. https://doi.org/10.1002/ajp.23384

Qi, X.-G., Wu, J., Zhao, L., Wang, L., Guang, X., Garber, P. A., Opie, C., Yuan, Y., Diao, R., Li, G., Wang, K., Pan, R., Ji, W., Sun, H. (2023). Adaptation to a Cold Climate Promoted Social Evolution in Asian Colobine Primates. Science, 380(1), 1-20. https://doi.org/10.1126/science.abl8621

Roos, C., & Zinner, D. (2022). Molecular Phylogeny and Phylogeography of Colobines. In Matsuda, I., Grueter, C.C., & Teichroeb, J.A. (Eds.) The Colobines: Natural History, Behaviour and Ecological Diversity (pp. 32–43). Cambridge : Cambridge University Press.

Sakti, A. D., Adillah, K. P., Santoso, C., Al Faruqi, I., Hendrawan, V. S. A., Sofan, P., Rustam, Fauzi, A. I., Setiawan, Y., Utami, I., Zain, A. F. M., & Kamal, M. (2024). Modeling Proboscis Monkey Conservation Sites on Borneo Using Ensemble Machine Learning. Global Ecology and Conservation, 54(1), 1-17. https://doi.org/10.1016/j.gecco.2024.e03101

Sanchez-Contreras, M., Sweetwyne, M. T., Kohrn, B. F., Tsantilas, K. A., Hipp, M. J., Schmidt, E. K., Fredrickson, J., Whitson, J. A., Campbell, M. D., Rabinovitch, P. S., Marcinek, D. J., & Kennedy, S. R. (2021). A Replication-Linked Mutational Gradient Drives Somatic Mutation Accumulation and Influences Germline Polymorphisms and Genome Composition in Mitochondrial DNA. Nucleic Acids Research, 49(19), 11103–11118. https://doi.org/10.1093/nar/gkab901

Sandel, A. A., Scott, J. E., & Kamilar, J. M. (2024). Primate Behavior and the Importance of Comparative Studies in Biological Anthropology. American Journal of Biological Anthropology, 186(78), 1-26. https://doi.org/10.1002/ajpa.70009

Santoso, N., Hasudungan, J. T., Sutopo, Hadiwijaya, I., Aripin, Ramadhan, Y., & Ridwan, S. M. (2023). Habitat Characteristics and Roaming Area of Proboscis Monkey in Bukit Semujan Swamp Forest Danau Sentarum National Park. Media Konservasi, 28(1), 24–34. https://doi.org/10.29244/medkon.28.1.24-34

Shao, Y., Zhou, L., Li, F., Zhao, L., Zhang, B.-L., Shao, F., Chen, J.-W., Chen, C.-Y., Bi, X., Zhuang, X.-L., Zhu, H.-L., Hu, J., Sun, Z., Li, X., Wang, D., Rivas-González, I., Wang, S., Wang, Y.-M., Chen, W., Li, G., Lu, H.-M., Liu, Y., Kuderna, L. F. K., Farh, K. K.-H., Fan, P.-F., Yu, L., Li, M., Liu, Z.-J., Tiley, G. P., Yoder, A. D., Roos, C., Hayakawa, T., Marques-Bonet, T., Rogers, J., Stenson, P. D., Cooper, D. N., Schierup, M. H., Yao, Y.-G., Zhang, Y-P., Wang, W., Qi, X.-G., Zhang, G., & Wu, D.-D. (2023). Phylogenomic Analyses Provide Insights into Primate Evolution. Science, 380(1), 913–924. https://doi.org/10.1126/science.abn6919

Tan, X., Qi, J., Liu, Z., Fan, P., Liu, G., Zhang, L., Shen, Y., Li, J., Roos, C., Zhou, X., & Li, M. (2023). Phylogenomics Reveals High Levels of Incomplete Lineage Sorting at the Ancestral Nodes of the Macaque Radiation. Molecular Biology and Evolution, 40(11), 1-20. https://doi.org/10.1093/molbev/msad229

Thakur, K., Sharma, D., Sharma, A., Sharma, A. K., Mahajan, D., Brar, B., Kumari, H., Kumar, S., Bala, M., Kumar, S., & Kumar, R. (2025). In Silico Analysis of Mitochondrial DNA Genes: Implication for Conservation of Tor Putitora (Hamilton, 1822). Scientific Reports, 15(1), 1-13. https://doi.org/10.1038/s41598-024-83669-w

Vanderpool, D., Minh, B. Q., Lanfear, R., Hughes, D., Murali, S., Harris, R. A., Raveendran, M., Muzny, D. M., Gibbs, R. A., Worley, K. C., Rogers, J., & Hahn, M. W. (2020). Primate Phylogenomics Uncovers Multiple Rapid Radiations and Ancient Interspecific Introgression. BioRxiv, 4(15), 1–49. https://doi.org/10.1101/2020.04.15.043786

Xie, J., Chen, Y., Cai, G., Cai, R., Hu, Z., & Wang, H. (2023). Tree Visualization by One Table (tvBOT): A Web Application for Visualizing, Modifying and Annotating Phylogenetic Trees. Nucleic Acids Research, 51(1), 587–592. https://doi.org/10.1093/nar/gkad359

Yu, J., Yu, X., Bi, W., Li, Z., Zhou, Y., Ma, R., Feng, F., Huang, C., Gu, J., Wu, W., Lan, G., Zhang, L., Chen, C., Xue, F., & Liu, J. (2025). Mitogenome Diversity and Phylogeny of Felidae Species. Diversity, 17(9), 1–15. https://doi.org/10.3390/d17090634

Zou, Y., Zhang, Z., Zeng, Y., Hu, H., Hao, Y., Huang, S., & Li, B. (2024). Common Methods for Phylogenetic Tree Construction and Their Implementation in R. Bioengineering, 11(5), 1-22. https://doi.org/10.3390/bioengineering11050480

Downloads

Published

2026-04-30

How to Cite

Sasmita, R., Badruzsaufari, B., & Pangestika, I. W. (2026). Insights into Evolutionary Relationships of Proboscis Monkeys Using In Silico Mitochondrial DNA Analysis. Biocaster : Jurnal Kajian Biologi, 6(2), 1153–1164. https://doi.org/10.36312/biocaster.v6i2.688

Issue

Section

Articles