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Table 4 Integration of gene expression with genetic modifiers

From: Integrated analysis of the aging brain transcriptome and proteome in tauopathy

Drosophila

Human

Gene

Amplifying vs. Protective

AD

Tangles

up-regulated

 cher

A

  

 Uba1

A

  

 Myd88

A

MYD88

 

 CG10889

A

ZC3H12C

 

 CG7970

A

  

 Elf

A

GSPT1

EIF2S1

 Fs(2)Ket

A

  

 Mekk1

A

  

 Nrg

A

CHL1

NRCAM

 smid

A

  

 Diap1

A

BIRC3

 

 wun

A

PLPP1

 

 Stip1

P

STIP1

 

 RpS21

P

RPS21

 

 Past1

P

EHD2

 

 Tis11

P

ZFP36L1, ZFP36L2

 

 w

P

  

 Gbs-70E

P

PPP1R3C

 

 cher

P

  

 dally

P

  

down-regulated

 fry

A

 

FRYL

 Ptp4E

A

  

 Atg6

A

  

 Fmr1

A

  

 mub

A

  

 Bacc

A

  

 jing

P

 

AEBP2

 E(bx)

P

 

BPTF

 tou

P

 

BAZ2B

 jar

P

  

 Mi-2

P

CHD5, CHD4

CHD4

 sgg

P

  

 milt

P

 

TRAK2

 stg

P

CDC25B

CDC25B

 twe

P

CDC25B

CDC25B

 Atx2

P

 

ATXN2L

 CG7231

P

  
  1. All Drosophila genes listed (at left) are modifiers of Tau-mediated neurodegeneration based on published unbiased screens [23,24,25]. Direction of Tau-induced differential expression is noted, including up- (top) or down-regulation (bottom) of transcripts. Based on the results of modifier tests, we can infer whether the observed Tau-induced expression perturbation is amplifying (A) or protective (P) for Tau neurotoxicity. See also Fig. 4 and Additional file 2: Table S9 and S10. For each fly gene, we also note whether human gene homolog(s) are differentially expressed in human postmortem brain tissue from published analyses of AD [10] and neurofibrillary tangle burden [11]. In cases where the direction of expression was concordant with Drosophila, the human gene name is indicated in boldface. In a smaller PSP dataset [9], only 1 fly gene, mub, had a differentially-expressed human homolog, PCBP4