Title: sequencing of the human -> functional genomics
1??4? ???
2??
- sequencing of the human -gt functional genomics
- Gene-expression microarrays and RNA interferences
(RNAi) - ATM/NF?B and ATM/p53-mediated arms
3functional genomics
- to gaining system-level understanding of the
mechanisms - gene products interact and regulate each other
- physiological processes during normal development
and in response to homeostatic challenges
4Gene-expression microarrays
- https//www.vbi.vt.edu/ article/articleview/145
5RNA interferences (RNAi)
(RNA-induced silencing complex)
- www.mpg.de/.../ EEB/200432_035.shtml
6RNA interferences (RNAi)
- www.life.uiuc.edu/ shapiro/RNAiApps.html
7ATM/p53 -mediatedATM/NFkB -mediated
G1 checkpoint
Ataxia- telangiectasia ( AT)
- www.biocarta.com/ pathfiles/m_atmPathway.asp
8NFkB
ATM/NFkB -mediated
- www.mbb.yale.edu/ fl/fl_s_ghosh.htm
9ATM
NFkB
ATM/NFkB -mediated
- http//www.emdbiosciences.com/popup/cbc/NFKB_Inter
active_Pathway.htm
10Hypothesis
- the combined experimental strategy of expression
arrays and RNAi is indeed a powerful method for
the dissection of complex transcriptional
networks, and that computational promoter
analysis can provide a strong complementary means
for assessing the accuracy of this dissection.
11?????
Definition of the damage-responding gene set
Microarray analysis
??siRNA knocked-downcellular systems
Computational promoter analysis
GO functional gene annotations
Cluster analysis
TRANSFAC
- New candidate target genes
Database search
Adapted from Thomas Werner Biomolecular
Engineering, 17 87-94 (2001)
12??siRNA knocked-downcellular systems
DNA fragments
To be cloned
pSUPER retroviral vector
To be transfected
HEK293 cell (????)
(selected with puromycin or hygromycin)
??????siRNA??,?????????????????????????,??????????
?????????,??????????? ???????????siRNA??,????????
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13?Western blotting ?? RNAi
- RNAi????????????,????????????
14Sample preparation and microarray hybridization
isolated using TRIzol reagent treated with DNase
I phenol/chloroform extracted ethanol-precipitated
and quantitated.
RNA
HEK293 cell
(4 h with 200 ng/ml of NCS.)
Affymetrix Human Focus Gene- Chip arrays
10 ??? five cellular systems (uninfected and
the LacZ control cells and cells knocked-down for
Rel-A, p53 and ATM), each probed at two time
points without treatment and 4 h after exposure
to NCS.
(All samples were probed in independent
triplicates)
15Computation of gene expression levels from
microarray signals
RMA method
1. RMA ???, ?????? 2. RMA ???????????????
16Definition of the damage-responding gene set
DMA method ???at least 1.5-fold in one control
(either the uninfected or the LacZ-infected
cells), and at least 1.4-fold in the same
direction in the other control.
A total of 112 genes that were induced in both
controls met this criterion and are referred to
as the damage-induced gene set. Only seven genes
met an analogous criterion for repression in
response to NCS treatment
17Cluster analysis
112 gene ?? the EXPANDER package ??
average-linkage hierarchical clustering
18GO functional gene annotations
The gene ontology (GO) annotations
Computational promoter analysis
PRIMA software
19Quantitative real-time RT-PCR
real-time PCR
cDNA
Five micrograms of total RNA
oligo(dT)
SuperScript II RNase H- reverse transcriptase
20(No Transcript)
21(No Transcript)
22??
- RNAi and microarray technologies and a recently
developed computational tool are powerful - off-target effects
- computational promoter analysis was highly
enriched for the binding signature of
ATF2/ATF3/Jun
23??
- RNAi, microarrays and computational promoter
analysis ?? dissection of transcriptional
networks ??????? - Targeting the primary activator of a DNA damage
response network, the upstream regulator(ATM) was
indeed required for the induction of much of the
network, the two downstream regulators
(p53/NFkB)mediated the activation of largely
disjoint sets of genes - Statistical tests ?? computational promoter
analysis ?????