12 research outputs found
Diverse Splicing Patterns of Exonized Alu Elements in Human Tissues
- Author
- A Gerber
- A Goren
- AG Clark
- AL Price
- Anne Tye
- AR Muotri
- AV Alekseyenko
- AV Alekseyenko
- B Mersch
- B Modrek
- B Moghadaszadeh
- Beverly L. Davidson
- BF Voight
- BJ Blencowe
- BR Graveley
- CG Goodyer
- CS Carlson
- D Karolchik
- ES Lander
- ET Wang
- F Tajima
- G Lev-Maor
- J Hasler
- J Piriyapongsa
- JA Calarco
- JA Lee
- James J. Cai
- JC Fay
- JL Kelley
- JM Akey
- K Kapur
- L Eng
- Lan Lin
- M Kreitman
- M Krull
- M Przeworski
- MW Pfaffl
- N Gal-Mark
- N Kim
- N Petit
- N Sela
- P Andolfatto
- P Yi
- PC Sabeti
- Peng Jiang
- PJ Gardina
- R Nielsen
- R Sorek
- R Sorek
- R Sorek
- RA Irizarry
- RC Lewontin
- RM Kuhn
- S Biswas
- S Olson
- S Rozen
- SB Hedges
- Shihao Shen
- SS Singer
- T Kwan
- TA Clark
- V Gotea
- W Makalowski
- WE Johnson
- WG Fairbrother
- WG Fairbrother
- XH Zhang
- Y Xing
- Y Xing
- Y Xing
- Yi Xing
- Yoshihide Hayashizaki
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2008
- Field of study
Exonization of Alu elements is a major mechanism for birth of new exons in primate genomes. Prior analyses of expressed sequence tags show that almost all Alu-derived exons are alternatively spliced, and the vast majority of these exons have low transcript inclusion levels. In this work, we provide genomic and experimental evidence for diverse splicing patterns of exonized Alu elements in human tissues. Using Exon array data of 330 Alu-derived exons in 11 human tissues and detailed RT-PCR analyses of 38 exons, we show that some Alu-derived exons are constitutively spliced in a broad range of human tissues, and some display strong tissue-specific switch in their transcript inclusion levels. Most of such exons are derived from ancient Alu elements in the genome. In SEPN1, mutations of which are linked to a form of congenital muscular dystrophy, the muscle-specific inclusion of an Alu-derived exon may be important for regulating SEPN1 activity in muscle. Realtime qPCR analysis of this SEPN1 exon in macaque and chimpanzee tissues indicates human-specific increase in its transcript inclusion level and muscle specificity after the divergence of humans and chimpanzees. Our results imply that some Alu exonization events may have acquired adaptive benefits during the evolution of primate transcriptomes
Pan-cancer analysis of whole genomes
- Author
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- Zhang
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- Zhang H. b
- Zhao
- Zheng
- Zhou
- Zhou
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- Zhu
- zi zj
- zm Jayaseelan
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- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
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Computational Design of Multi-component Bio-Inspired Bilayer Membranes
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Heat shock factor 2 is required for maintaining proteostasis against febrile-range thermal stress and polyglutamine aggregation
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- Abane R
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- Akira Nakai
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- 'American Society for Cell Biology (ASCB)'
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- Field of study
Functional consequences of developmentally regulated alternative splicing
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- A Kalsotra
- A Kalsotra
- A Rosa
- AE McKee
- AJ Lopez
- AK Ramani
- AL Saltzman
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- Auinash Kalsotra
- B Modrek
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- C Ghigna
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- D Hattori
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- D LaGamba
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- D Mordes
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- DA Zacharias
- DD Licatalosi
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- DS Chandler
- E Melamud
- E Theodorou
- EJ Wagner
- EM Munding
- EN Olson
- ET Wang
- EV Makeyev
- EY Ahn
- F Heyd
- F Tang
- F Tang
- FW Scherrer Jr.
- G Biamonti
- G Neves
- G Ohno
- GW Yeo
- GW Yeo
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- H Keren
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- H Lin
- H Ponta
- H Seitz
- H Takechi
- HJ Yost
- I Voineagu
- J Engebrecht
- J Han
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- J Xie
- J Xie
- J Yang
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- JA Calarco
- JA Calarco
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- JA Pleiss
- JC Long
- JH Ding
- JK Pickrell
- JP Thiery
- JP Thiery
- JQ Wu
- JT Witten
- JW Park
- JY Ip
- JZ Ni
- K Bhalla
- K Juneau
- K Polyak
- KK Tomczak
- L De Moerlooze
- LA Boyer
- LE Maquat
- LF Lareau
- LT Gehman
- M Ares Jr
- M Chen
- M Corioni
- M Dutertre
- M Fagnani
- M Gabut
- M Irimia
- M Koshelev
- M Pritsker
- M Ruggiu
- M Spingola
- M Stadtfeld
- M Yano
- MB Gerstein
- MH Soonpaa
- MJ Moore
- MJ Moore
- MJ Munoz
- MP Paronetto
- N Cloonan
- N Salomonis
- N Salomonis
- NJ McGlincy
- O Isken
- P An
- PL Boutz
- Q Li
- Q Pan
- R Brandenberger
- R Karni
- R Spellman
- RB Darnell
- RF Luco
- RF Luco
- RL Brown
- RN Kanadia
- S Komili
- S Rao
- SG Amara
- T Maniatis
- TA Clark
- Thomas A. Cooper
- TW Nilsen
- X Li
- X Wang
- X Wang
- X Xu
- XL Zhan
- XY Zhong
- Y Barash
- Y Feng
- Y Haupt
- Y Mayshar
- Y Xing
- Y Yu
- YY Yang
- Z Chen
- ZR Qiu
- ZR Qiu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study