고려 인삼(Panax ginseng)의 뿌리로부터 ribulose-1,5-bisphosphate carboxylase small subunit(rbcS) 유전자를 선발하여 sequence 분석을 실시하였다. 고려 인삼 rbcS cDNA는 790 bp 염기로 구성되어 있으며, 183개의 아미노산(pI 8.37)을 코드하는 549 bp의 ORF를 가지고 있고 단백질의 분자량은 20.5 kDa으로 추정되었다. 인삼 rbcS는 기존에 보고된 것과 유사성을 나타내었으며, Helianthus annuus(CAA68490)에서 분리된 것과 78%의 높은 상동성을 보였다. 기존에 데이터베이스에 축적되어 있는 다른 식물체로부터 분리된 rbcS와 아미노산 서열을 비교한 결과 인삼의 ybcS는 H. annuus (CAA68490), C. morifolium (AAO25119), L. sativa (Q40250)와 밀접한 유연관계에 있는 것으로 조사되었다.

A class I type 2 metallothionein (CMet2) cDNA from taproot of Codonopsis lanceolata was isolated and characterized. A CMet2 cDNA was 572 nucleotides long and had an open reading frame of 234 bp with a deduced amino acid sequence of 78 residues (pI = 4.99). The deduced amino acid sequence of CMet2 matched to the previously reported type 2 metallothionein-like protein genes and showed 74% identity with that of G. max (BAD18377) and C. arietinum (CAA65009). Expression of CMet2 by the RT-PCR was increased at 1 hr after cadmium and hydrogen peroxide treatment, respectively.

A full-length cDNA (PPrx1) encoding peroxidase has been isolated and its nucleotide sequence determined from flower bud in ginseng plant (Panax ginseng). A PPrx1 cDNA is 1192 nucleotides long and has an open reading frame of 1062 bp with a deduced amino acid sequence of 354 residues (pI 7.53). The deduced amino acid sequence of PPrx1 matched to the previously reported peroxidase protein genes. The PPrx1 showed a high similarity with the 64% identity with peroxidase of N. tabacum (AAK52084). In the phylogenetic analysis based on the amino acid residues, the PPrx1 was closer with peroxidase of G. max (AAD37376).

The sex differentiation of fishes occurs under the control of genetic and various environmental factors. DM-domain containing genes are novel zinc finger transcription factors and play key roles in sex determination. In order to isolate the wrasse DMRT (wDMRT) cDNA from the protogynous wrasse (Halichoeres tenuispinnis), the wrasse testis cDNA library was screened using the P-labeled PCR products, which were amplified with the degenerate primers from conserved DM-domain regions of several DMRT genes. Among a few positives obtained through screening, the full length wDMRT cDNA of 2.9kb size encoding a predicted 300 amino acid residues was isolated. The sequence analysis exhibited 60%, 43% sequence identity with rainbow trout and tilapia DMRT1, respectively. RT-PCR assay showed that wDMRT was expressed specifically in male testis. Also, wDMRT gene was strongly expressed in May during reproductive season, when the reproductivity of wrasse is most active. This results suggested that wDMRT gene function in testis differentiation The conserved DM-domain regions were amplified using PCR from DMRT genes of several species among Labridae, and their sequences were determined. The sequence of DM-domain region of Halichoeres. tenuispinis was identical to those of Pseudolabrus japonicus, Pteragogus flagellifera, and showed 94% identity with that of Halichoeres poecioptrerus.

점액질이 풍부한 꼼치 조직에서 NIH 3T3 세포주를 이용하여 subtracted cDNA 라이브러리를 얻어 200례의 클론을 제작하였다. 이 클른 중에서 비반복성 유전자를 선택하고, RNA in situ hybridization을 실행하여 꼼치 조직에서 특이하게 발현되는 곰신 클론(C90-171)을 선택하였다. 이 클론은 사람의 타액선 조직에서도 특이하게 발현되는 유전자로서 이를 확인하기 위하여 C90-171(곰신) 항체를 제작하였다. 꼼치의 cDNA

심해에서 서식하며 특이한 조직형태를 갖고 있는 꼼치조직에서 cDNA를 제작하여 클로닝을 통해서, 꼼치에서 특이하게 발현하는 유전인자를 검색하였다. 그 결과 62례의 클론이 알려진 유전자에 동질성이 있었는데 이들은 thioesterase가 9례, myosin이 8례, creatine kinase가 7례, skeletal alpha-actin이 6례, parvalbumin b와 ribosomal protein이 각각 5례, type I collagen과 m