Sains Malaysiana 55(9)(2026): 1441-1453

http://doi.org/10.17576/jsm-2026-5509-03

 

Sex-Specific Transcriptomic Profiling of the Perfectly Synchronous Flashing Fireflies Pteroptyx tener (Coleoptera, Lampyridae)

(Pemprofilan Transkriptomik Khusus Jantina bagiKelipan Sinkroni SempurnaKelip-Kelip Pteroptyx tener (Coleoptera, Lampyridae))

 

AMIRAH MOHAMMAD-SIDIK1,2, NUR KHAIRUNNISA SALLEH1, KOK KEONG LOKE2, NORELA SULAIMAN1, MOHD FIRDAUS-RAIH2,3,4,5 & CHYAN LEONG NG2,5,6,*

 

1Department of Biological Sciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia

2Institute of Systems Biology (INBIOSIS), Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia

3Department of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia
4Bioinformatics and Molecular Simulations Research Group, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia
5Structural Biology and Protein Engineering Research Group, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia
6Systems and Synthetic Biology Research Group, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor, Malaysia

Received: 31 October 2025/Accepted: 19 August 2026

 

*Corresponding author; email: clng@ukm.edu.my

 

Abstract

The firefly species Pteroptyx tener is well known for its precisely synchronous male flashing behaviour at night, while females do not exhibit this trait. However, the molecular mechanisms underlying this synchronisation by males remain largely unknown. To understand the genetic basis of this firefly synchronous flashing, RNA sequencing (RNA-seq) was performed on samples from males and females of P. tener collected during the day and at night, generating approximately 43 to 50 million reads per sample with over 90% of bases achieving a Phred quality score above 30. Due to the lack of a reference genome for this species, de novo assembly of the sequencing data was conducted resulting in 160,894 total transcripts. Raw data (FASTQ) were deposited in the NCBI Sequence Read Archive (SRA) with the accession number PRJNA1242504. The discovery of a hidden-break in 28S rRNA highlighted the need for revised RNA integrity assessment protocols for arthropod species, as standard RIN-based metrics might yield misleading results. Differential expression analysis showed a list of 151 genes consistently upregulated in male night samples compared to all other groups under a false discovery rate p-value threshold of less than 0.05. Within this group, the top 20 upregulated genes exhibited maximum log2 fold change values between 10 and 12. The study indicated that the overall transcriptomic profile in P. tener was influenced by sex rather than by sampling time. This finding suggests potential sex-specific regulation of genes involved in bioluminescence and signalling. This identification of differentially expressed genes and key molecular pathways is potentially crucial for the firefly species with synchronous flashing behaviour, offering new avenues for future functional and evolutionary studies on firefly communication. Additionally, it offers insights into sex-specific transcriptomic differences that may influence other biological processes in P. tener.

Keywords: Fireflies; Pteroptyx tener; RNA-seq; sex; synchronous flashing

 

Abstrak

Kelip-kelip jantan species Pteroptyx tener terkenal dengan ciri kelipan sinkroni pada waktu malam, manakala kelip-kelip betina tidak menunjukkan ciri tersebut. Namun begitu, mekanisme molekul yang mendasari kelipan sinkroni oleh jenis jantan masih belum diketahui dengan jelas. Bagi memahami asas genetik kelipan sinkroni kelip-kelip, penjujukan RNA (RNA-seq) telah dijalankan ke atas sampel jantan dan betina P. tener yang diambil pada waktu siang dan malam, menghasilkan kira-kira 43 hingga 50 juta bacaan setiap sampel dengan lebih 90% bes mencapai skor kualiti Phred melebihi 30. Disebabkan ketiadaan genom rujukan bagi spesies ini, himpunan semula data penjujukan secara de novo telah dilakukan yang menghasilkan 160,894 transkrip. Data mentah (FASTQ) telah disimpan dalam NCBI Sequence Read Archive (SRA) dengan nombor akses PRJNA1242504. Penemuan pecahan tersembunyi pada 28S rRNA menekankan keperluan untuk menyemak semula protokol penilaian kualiti RNA bagi spesies artropod, kerana metrik berasaskan RIN semata-mata mungkin memberikan keputusan yang mengelirukan. Analisis pembezaan pengekspresan menyenaraikan 151 gen dengan pengekspresan yang tinggi dalam sampel jantan pada waktu malam berbanding semua sampel lain dengan nilai p kadar penemuan palsu kurang daripada 0.05. Dalam kumpulan sampel ini, 20 gen teratas yang diekspreskan dengan tinggi menunjukkan nilai perubahan log2 kali ganda maksimum antara 10 hingga 12. Kajian ini menunjukkan bahawa profil transkriptom keseluruhan P. tener lebih dipengaruhi oleh faktor jantina berbanding masa pensampelan. Keputusan ini mencadangkan kemungkinan wujudnya pengawalaturan khusus jantina bagi gen yang terlibat dalam biopendarkilau dan pengisyaratan. Pengenalpastian gen yang diekspreskan secara berbeza dan tapak jalan molekul utama ini penting untuk spesies kelip-kelip yang mempunyai sifat sinkroni kelipan bagi membuka peluang baharu untuk kajian fungsian dan evolusi komunikasi kelip-kelip pada masa hadapan. Tambahan pula, keputusan ini turut memberikan pandangan baharu terhadap perbezaan transkriptom khusus jantina yang mungkin mempengaruhi proses biologi lain dalam P. tener.

Kata kunci: Jantina; kelipan sinkroni; kelip-kelip; penjujukan RNA; Pteroptyx tener

 

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