| Sains  Malaysiana 34(1): 27-32 (2005)    Pembinaan dan Pencirian  Perpustakaan Genom Siakap (Lates  calcarifer) (Construction and Characterisation of Genomic Library  for Sea bass Lates calcarifer)     Pan-Pan Chong, Adura Mohd-Adnan & Kiew-Lian Wan Pusat Pengajiain BioSains dan Bioteknologi Fakulti Sains dan Teknologi Universiti Kebangsaan Malaysia 43600 UKM Bangi, Selangor, Malaysia       ABSTRAK   Siakap  (Lates calcarifer) merupakan spesies ikan yang penting dari segi ekonomi  di Malaysia. Dalam kajian ini, satu perpustakaan genom L. calcarifer telah dibina. DNA genom telah dipencil daripada tisu otot L. calcarifer,  diserpih secara nebulisasi, dibaiki hujung tumpul dan diligasi ke dalam vektor  plasmid pCR®4Blunt-TOP®. Campuran ligasi seterusnya telah ditransformasikan ke  dalam Escherichia coli. Bagi mencirikan perpustakaan genom yang  terhasil, DNA plasmid telah diekstrak daripada klon-klon rekombinan yang  dipilih secara rawak. Elektroforesis gel agaros menunjukkan klon-klon  rekombinan ini membawa selitan DNA yang bersaiz di antara 0.5 kb - 3.5 kb, dengan purata saiz 1.7 kb. Seterusnya, penjujukan DNA telah  dijalankan dengan menggunakan DNA plasmid yang diperoleh sebagai templat.  Sebanyak 121 jujukan rawak telah dihasilkan daripada perpustakaan genom L.  calcarifer ini. Analisis jujukan rawak memberikan implikasi yang  perpustakaan ini adalah representatif bagi genom L. calcarifer.  Berdasarkan persamaan dengan jujukan dalam pangkalan data, 17% jujukan rawak  ini didapati mempunyai keputusan BLAST yang bermakna, yang menunjukkan mereka  mewakili gen L. calcarifer. Analisis dengan menggunakan perisian  RepeatMasker menunjukkan sebanyak 25% jujukan rawak ini dikenal pasti sebagai  unsur berulang. Pencirian awal terhadap perpustakaan genom ini menunjukkan ia  berpotensi sebagai sumber yang berguna dalam kajian genom L. calcarifer.    Kata  kunci: Perpustakaan Genom, Lates calcarifer      ABSTRACT   Sea  bass (Lates calcarifer) is an economically important fish in Malaysia.  In this study, a genomic library of L. calcarifer was constructed.  Genomic DNA was isolated from the muscle tissue of sea bass, sheared by  nebulisation, blunt-end repaired and ligated into the pCR®4Blunt- TOPO® plasmid  vector. The ligation mixture was then transformed into Escherichia coli. In  order to characterize the constructed genomic library, plasmid DNA was  extracted from randomly selected recombinant clones. Gel electrophoresis showed  that these recombinant clones contain inserts with a size range of 0.5 kb - 3.5 kb, with an average size of 1.7 kb. DNA sequencing was then carried out  using the extracted DNA plasmid as template, and a total of 121 random  sequences were generated from the L. calcarifer genomic library.  Analysis of these sequences implies that the library is representative of L.  calcarifer genome. Based on sequence similarity database searches, 17% of  the random sequences were found to have significant BLAST hits, indicating that  they represent L. calcarifer genes. Analysis using the Repeat Masker  program reveals that 35% of the random sequences were identified as repeat  elements. Initial characterization of this genomic library indicates that it is  a potentially useful resource in the study of the L. calcarifer genome.    Keywords:  Genomic library, Lates calcarifer      RUJUKAN/REFERENCES   Altschul, S. F, Madden, T. L. Schaffer,  A. A., Zhang, J., Zhang, Z., Miller, W. &  Lipman, D. J. 1997. Gapped BLAST and PSIBLAST: a new generation of  protein database search programs. 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