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. Author manuscript; available in PMC: 2012 Feb 13.
Published in final edited form as: Nat Cell Biol. 2011 Feb 20;13(3):203–214. doi: 10.1038/ncb2163

Table 1.

Most early transcriptional changes in basal cells depleted of Srf involve regulators of actomyosin and not cell cycle, inflammation, ABP or Notch signalling genes.

Actomyosin Fblim1(−3.7)* Cnn2(−3.1)* Actb(−2.0)* Flna(−1.8)* Arhgap24(−1.8)* Actg1(−1.7)* Wdr1(−1.6)* Pfn2(−1.3)* Gsn(−1.3)*
cytoskeleton Myh9 Myh10 Myh14 Myl9
Cell adhesion Gjb5(−2.6)* Pcad20(−2.2)* Dsg1b(−1.8)* Tns4(−1.6)* Cdh1 Ctnna1 Ctnnb1 Tjp1 Tjp2 Ocln Itgb1
Immediate
early genes
Egr2(−8.6)* Egr1(−5.0)* Egr3(−3.9)* Fos Junb
Immune
response
Il1b Il6 Il18 Ccl2 Ccl27a S100a8 S100a9
Cell cycle Mki67 Ccna1 Ccna2 Ccnb1 Ccnb2 Ccnd1 Ccnd2(1.5) Ccnd3 Ccne1 Ccne2
Notch signalling Notch1 Notch2 Notch3 Jag1 Jag2 Dll1
Apico-basal Pard3 Pard3b Pard6a Pard6b Pard6g Prkcc Prkcz
polarity

Embryos were from K14–Cre×Rosa26YFP fl/fl ×Srf fl/fl (wild-type and cKO littermates). Basal cells active for Cre recombinase expressed YFP and were enriched for surface α6-integrin. After FACS purification, mRNAs were subjected in duplicate for microarray analyses. Data from two independent arrays revealed 72 mRNAs that scored as up- or downregulated by at least 1.5-fold with P <0.05. DAVID clustering analyses showed that the affected process is the actomyosin cytoskeleton, whereas ABP, Notch, cell cycle regulators and pro-inflammation associated genes showed no change at this early time.

*

Decrease in early (E16.5) mRNA expression

No change in early (E16.5) mRNA expression

Increase in early (E16.5) mRNA expression