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sequencing of the human -> functional genomics

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4 sequencing of the human - functional genomics Gene-expression microarrays and RNA interferences (RNAi) ATM/NF B and ATM/p53-mediated ... – PowerPoint PPT presentation

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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

3
functional 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

4
Gene-expression microarrays
  • https//www.vbi.vt.edu/ article/articleview/145

5
RNA interferences (RNAi)
(RNA-induced silencing complex)
  • www.mpg.de/.../ EEB/200432_035.shtml

6
RNA interferences (RNAi)
  • www.life.uiuc.edu/ shapiro/RNAiApps.html

7
ATM/p53 -mediatedATM/NFkB -mediated
G1 checkpoint
Ataxia- telangiectasia ( AT)
  • www.biocarta.com/ pathfiles/m_atmPathway.asp

8
NFkB
ATM/NFkB -mediated
  • www.mbb.yale.edu/ fl/fl_s_ghosh.htm

9
ATM
NFkB
ATM/NFkB -mediated
  • http//www.emdbiosciences.com/popup/cbc/NFKB_Inter
    active_Pathway.htm

10
Hypothesis
  • 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
  • Materials and methods

DNA fragments
To be cloned
pSUPER retroviral vector
To be transfected
HEK293 cell (????)
(selected with puromycin or hygromycin)
??????siRNA??,?????????????????????????,??????????
?????????,??????????? ???????????siRNA??,????????
??????
13
?Western blotting ?? RNAi
  • RNAi????????????,????????????

14
Sample preparation and microarray hybridization
  • Materials and methods

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)
15
Computation of gene expression levels from
microarray signals
  • Materials and methods

RMA method
1. RMA ???, ?????? 2. RMA ???????????????
16
Definition of the damage-responding gene set
  • Materials and methods

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
17
Cluster analysis
  • Materials and methods

112 gene ?? the EXPANDER package ??
average-linkage hierarchical clustering
18
GO functional gene annotations
  • Materials and methods

The gene ontology (GO) annotations
Computational promoter analysis
  • Materials and methods

PRIMA software
19
Quantitative real-time RT-PCR
  • Materials and methods

real-time PCR
cDNA
Five micrograms of total RNA
oligo(dT)
SuperScript II RNase H- reverse transcriptase
20
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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 ?????
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