The study aims to determine the genetic character of Black-capped white-eye (Zosterops articapilla) using the mtDNA COI gene. Blood sample was collected from bird market in Bengkulu city and its DNA genome isolation and purification following the Protocols of Dneasy® Blood and Tissue Kit Cat no 69504 (50) based on the procedure of Spin-Column Protocol, Qiagen. We used polymerase chain reaction machine for amplification DNA template with specific primer (ZCOIF and ZCOIR). The results showed that there are nucleotide variations on five individual Black-capped white-eye with the COI gene sequence length 750 bp. We found of conservative site (C) is 743 sites, variations (V) seven sites, parsimony (Pi) four sites, singleton (S) three sites, and nucleotide base pairs of Zosterops atricapilla to adenine and thymine (AT) 55.9% and guanine and cytosine (GC) 44.1%. Fifth individual of Black-capped white-eye are separated with average intraspecies genetic distance 0.4%, while its interspecific genetic distance is 3.47% and with the outgroup 12.1%. We think, these COI gene sequences very important to quick identification and could be used as a forensic tool in preventing its trafficking.

Abstract. Jarulis, Muslim C, Kamilah SN, Utama AF, Permana D, Sari MM, Prayitno AH, Jannah IM. 2021. DNA barcode of Enggano hill myna, Gracula religiosa enganensis (Aves: Sturnidae) based on mitochondrial DNA cytochrome oxidase subunit I. Biodiversitas 22: 1635-1643. The sharp decline of the Enggano hill myna population due to illegal trading and habitat degradation needs to be our concern to prevent this bird from extinction. Taxonomically, Enggano hill myna is referred to as a sub-species, but this has not been confirmed by genetic data. We have sequenced seventeen Enggano hill myna mitochondrial DNA COI genes to describe their genetic identity (barcode), genetic distances, and phylogeny. DNA genome from seventeen blood samples was isolated with DNeasy® Blood and Tissue Kit Qiagen, while PCR amplification was performed using a pair primers, namely COIGRF (5'-TTCTGATTCTTTGGCCATCC-3') and COIGRR (5'-GTTGGAAGGCTTTGCGTTTA-3'). We used Clustal W alignment in MEGA 10.2.2 software to search single nucleotide polymorphisms. Genetic distance was analyzed by using the Kimura 2-parameter, and the phylogenetic tree was reconstructed with Neighbor-Joining models. We found 98.60% conservative sites, 0.69% parsimony sites, and 0.83% singleton sites from the 716 bp sequence. The highest nucleotide composition was cytosine (32.20%), and the lowest was guanine (16.80%), followed by 49% GC content. Seven SNP sites were found in 716 bp COI gene sequences of seventeen individuals. The genetic distance between Enggano hill myna individuals was ranged from 0.0-0.8%, and all Enggano hill myna individuals separated from Chinese and Indian populations in the phylogenetic tree with a genetic distance of 0.9% and 1.1%. Our data suggest that the Enggano hill myna population is still classified as a sub-species. The COI gene sequences that we found can be used to quickly identify this species and are also important to prevent illegal trading in Indonesia.