abstract

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ABSTRACT Transposable elements are the most abundant interspersed sequences in human genome. It has been estimated that approximately 45% of the human genome comprises of transposable elements. Most of transposable elements are transcriptionally silent in human normal tissues, however, some of transposable elements have been found to be expressed in placenta tissues and cancer cell lines. Recent studies have shown that transposable elements could affect coding sequences, splicing patterns, and transcriptional regulation of human genes. In the present study, we investigated the transposable elements in relation to human cancer. Our analysis pipeline adopted for screening methods of the cancer specific expression from human expressed sequences. We developed a database for understanding the mechanism of cancer development in relation to transposable elements. Totally, 999 genes were identified to be integrated in their mRNA sequences by transposable element. We believe that our work might help many scientists who interested in cancer research to gain the insight of transposable element for understanding the human cancer.. INTRODUCTION & RESEARCH AIMS Most of TEs are transcriptionally silent in human normal tissues, however, some of TEs have been found to be expressed in placenta tissues and cancer cell lines. The L1 antisense promoter-driven transcription has been detected in human tumor cells or normal ones, while HERV LTR elements have shown the bidirectional promoter activity (Medstrand et al., 2001; Nigumann et al., 2002; Dunn et al., 2003; Sin et al., 2006). Those elements could provide biological role of organismal complexity by transcriptional diversity (Landry et al., 2003). Here, we developed a database for understanding the mechanism of cancer development in relation to TEs in human EST sequences. MATERIALS & METHODS SUMMARIES AND FUTURE DIRECTIONS Through this update, we will be able to profile the patterns of transposable expression in various diseases and to understand the transposable element that have an effect on the expression of human functional genes. We believe that our work will help us gain insight into implication of TEs expression in human evolution and diseases. RESULTS & DISCUSSION http://www.primate.or.kr REFERENCES Kim TH, Jeon YJ, Kim WY, Kim HS: HESAS: HERVs expression and structure analysis system Bioinformatics 2005, 15:1699-1970. Kim DS, Kim TH, Huh JW, Kim IC, Kim SW, Park HS, Kim HS : LINE FUSION GENES: a databas of LINE expression in human genes. BMC Genomic 2006, 7:139 13.6% 3.8% 1.6% 0.7% 0.2% 0.1% 0.1% 79.8% 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 1 2 3 4 5 6 11 17 Transposable elem entfuion EST counts G enes% Figure Transposable elements fusion EST counts 11% 82% 6% 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 5′U TR CDS 3′U TR Location oftransposable elem ents fusion EST Percentofexons% Transposable elem ents fusion region w ithin genes SIN E Fam ily LIN E Fam ily LTR Fam ily DNA Fam ily O thers CDS 619 280 85 76 1 5′U TR 76 30 33 5 0 3′U TR 44 20 14 5 0 Transposable elem ents Table D istribution oftransposable elem entfam ily in region oftransposable elem entexonization 5U TR CDS 3UTR Alu 0 20 0 AluJ 20 131 12 AluS 13 190 15 AluY 3 37 5 MIR 33 198 7 FA M 0 2 0 FRAM 0 16 2 FLA M 7 25 3 HAL 0 11 0 L1H S 0 1 0 L1P 1 12 5 L1M 6 125 6 L2 22 111 7 L3 1 20 2 M aLR 16 40 6 ERV1 13 23 3 ERVL 4 16 5 ERVK 0 6 0 Charlie 0 9 0 HSM AR2 0 2 0 K anga1 0 0 1 M ARNA 0 3 0 M ER 5 50 3 Tigger 0 11 1 Zaphod2 0 1 0 O thers Charlie 0 1 0 Transposable elem entsfusion in gene region DNA Fam ily LTR Fam ily LIN E Fam ily SIN E Fam ily Family Subfamily Table Distribution of transposable elements into coding and untranslated region of gene Table 3 EST based expression profiles of transposable elements in human cancer Type of potentialsplicing site SIN E Fam ily LIN E Fam ily LTR Fam ily DNA Fam ily A ccept& D onor 83 68 50 12 A cceptSite 271 110 33 28 DonorSite 216 80 43 18 Transposable elem ents Table Potentialsplice site are utilized by transposable elem entsfusion exons Database Construction Dae-Soo Kim 1 , Un-Jong Jo 1 ,Jae-Won Huh 2 and Heui-Soo Kim 1, 2 1 PBBRC, Interdisciplinary Research Program of Bioinformatics, College of Natural Sciences, Pusan National University, Busan 2 Division of Biological Sciences, College of Natural Sciences,Pusan National University, Busan http:// www.primate.or.kr/ oo Kim 1 ,Jae-Won Huh 2 and Heui-Soo Kim 1, 2 C, Interdisciplinary Research Program of Bioinformatics, College of Natural Sciences, National University, Busan sion of Biological Sciences, College of Natural Sciences,Pusan National University, Busan Bioinformatic Discovery of TransposableElements Expression in Human Cancer Molecular Biology & Phylogeny LAB. Genome Information LAB & Primate & Long Terminal Repeat & Long Interspersed Nuclear Elements & Short Interspersed Nuclear Elements

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Dae-Soo Kim 1 , Un-Jong Jo 1 ,Jae-Won Huh 2 and Heui-Soo Kim 1, 2 1 PBBRC, Interdisciplinary Research Program of Bioinformatics, College of Natural Sciences, Pusan National University, Busan 2 Division of Biological Sciences, College of Natural Sciences,Pusan National University, Busan. - PowerPoint PPT Presentation

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Page 1: ABSTRACT

ABSTRACTTransposable elements are the most abundant interspersed sequences in human genome. It has been estimated that approximately 45% of the human genome comprises of transposable elements. Most of transposable elements are transcriptionally silent in human normal tissues, however, some of transposable elements have been found to be expressed in placenta tissues and cancer cell lines. Recent studies have shown that transposable elements could affect coding sequences, splicing patterns, and transcriptional regulation of human genes. In the present study, we investigated the transposable elements in relation to human cancer. Our analysis pipeline adopted for screening methods of the cancer specific expression from human expressed sequences. We developed a database for understanding the mechanism of cancer development in relation to transposable elements. Totally, 999 genes were identified to be integrated in their mRNA sequences by transposable element. We believe that our work might help many scientists who interested in cancer research to gain the insight of transposable element for understanding the human

cancer..

INTRODUCTION & RESEARCH AIMSMost of TEs are transcriptionally silent in human normal tissues, however, some of TEs have been found to be expressed in placenta tissues and cancer cell lines. The L1 antisense promoter-driven transcription has been detected in human tumor cells or normal ones, while HERV LTR elements have shown the bidirectional promoter activity (Medstrand et al., 2001; Nigumann et al., 2002; Dunn et al., 2003; Sin et al., 2006). Those elements could provide biological role of organismal complexity by transcriptional diversity (Landry et al., 2003). Here, we developed a database for understanding the mechanism of cancer development in relation to TEs in human EST sequences.

MATERIALS & METHODS

SUMMARIES AND FUTURE DIRECTIONSThrough this update, we will be able to profile the patterns of transposable expression in various diseases and to understand the transposable element that have an effect on the expression of human functional genes. We believe that our work will help us gain insight into implication of TEs expression in human evolution and diseases.

RESULTS & DISCUSSIONhttp://www.primate.or.kr

REFERENCESKim TH, Jeon YJ, Kim WY, Kim HS: HESAS: HERVs expression and structure analysis system. Bioinformatics 2005, 15:1699-1970.

Kim DS, Kim TH, Huh JW, Kim IC, Kim SW, Park HS, Kim HS : LINE FUSION GENES: a databaseof LINE expression in human genes. BMC Genomic 2006, 7:139

13.6%

3.8%1.6% 0.7% 0.2% 0.1% 0.1%

79.8%

0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

1 2 3 4 5 6 11 17

Transposable element fuion EST counts

Gen

es %

Figure Transposable elements fusion EST counts

11%

82%

6%

0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

5′UTR CDS 3′UTR

Location of transposable elements fusion EST

Per

cent

of

exon

s %

Transposable elements fusion region within genes SINE Family LINE Family LTR Family DNA Family Others

CDS 619 280 85 76 1

5′UTR 76 30 33 5 0

3′UTR 44 20 14 5 0

Transposable elements

Table Distribution of transposable element family in region of transposable element exonization

5UTR CDS 3UTR

Alu 0 20 0

AluJ 20 131 12

AluS 13 190 15

AluY 3 37 5

MIR 33 198 7

FAM 0 2 0

FRAM 0 16 2

FLAM 7 25 3

HAL 0 11 0

L1HS 0 1 0

L1P 1 12 5

L1M 6 125 6

L2 22 111 7

L3 1 20 2

MaLR 16 40 6

ERV1 13 23 3

ERVL 4 16 5

ERVK 0 6 0

Charlie 0 9 0

HSMAR2 0 2 0

Kanga1 0 0 1

MARNA 0 3 0

MER 5 50 3

Tigger 0 11 1

Zaphod2 0 1 0

Others Charlie 0 1 0

Transposable elements fusion in gene region

DNA Family

LTR Family

LINE Family

SINE Family

Family Subfamily

Table Distribution of transposable elements into coding and untranslated region of gene

Table 3 EST based expression profiles of transposable elements in human cancer

Type of

potential splicing site SINE Family LINE Family LTR Family DNA FamilyAccept&Donor 83 68 50 12Accept Site 271 110 33 28Donor Site 216 80 43 18

Transposable elements

Table Potential splice site are utilized by transposable elements fusion exons

Database Construction

Dae-Soo Kim1, Un-Jong Jo1,Jae-Won Huh2 and Heui-Soo Kim1, 2

1PBBRC, Interdisciplinary Research Program of Bioinformatics, College of Natural Sciences, Pusan National University, Busan2Division of Biological Sciences, College of Natural Sciences,Pusan National University, Busan

http://www.primate.or.kr/

Dae-Soo Kim1,Jae-Won Huh2 and Heui-Soo Kim1, 2

1PBBRC, Interdisciplinary Research Program of Bioinformatics, College of Natural Sciences, Pusan National University, Busan2Division of Biological Sciences, College of Natural Sciences,Pusan National University, Busan

Bioinformatic Discovery of TransposableElements Expression in Human Cancer

Molecular Biology & Phylogeny LAB.

Genome Information LAB & Primate & Long Terminal Repeat & Long Interspersed Nuclear Elements & Short Interspersed Nuclear Elements