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1 doi: /nature07173 SUPPLEMENTARY INFORMATION Supplementary Figure Legends: Supplementary Figure 1: Model of SSC and CPC divisions a, Somatic stem cells (SSC) reside adjacent to the hub (red), self-renew and produce both hub cells and cyst cells. Cyst progenitor cells (CPC) are further away from the hub and divide to produce early cyst cells (ecc) that will encapsulate the dividing germ cells. b, Prediction of labeled somatic cell types. SSCs and CPCs are mitotically active cells (asterisks) whose daughters can be labeled during mitotic recombination. Predicted frequencies were calculated using experimental data of mitotic somatic cells (see text). SSCs (69% of mitotic somatic cells) can generate SSCs, hub cells, and CPCs. Assuming an equal probability of labeling a SSC (33%), hub cell (33%), or CPC (33%) during mitotic recombination, the frequency of labeled cells resulting from SSC division can be calculated: 69% x 33% = 22.8%. The frequency of labeled early cyst cells, the result of a CPC division (31% of mitotic somatic cells), can also be calculated: 31% x 100% = 31%. Predictions are similar to observed frequencies at 1-day post heat shock from testes containing clones (SSC, 22.5%; hub cell, 16.8%; CPC, 20.2%; early cyst cell, 32.6%) (see below and Figure 3f). c, Table with frequencies of marked (β-gal+) somatic cell types in testis containing a marked (β-gal+) cell at 1, 5, 10, 15 or 50 days post heat shock (DPHS). Sample numbers are provided in parentheses. 1
2 doi: /nature07173 SUPPLEMENTARY INFORMATION Supplementary Figure 2. shotgun (shg) function is required for maintenance of male GSCs. a-f, Fluorescence images of Drosophila testes. a,d, GFP negative, GSC control clones are evident by two days post heat shock (DPHS) and maintained at ten DPHS in (outlined) y,w, hsflp 122 ; FRTG13/FRTG13,GFP males. GFP negative shg mutant GSC clones are generated using (b) shg IG29 and (c) shg IH loss of function alleles that are lost by 10 DPHS (e,f). g, Graphical representation of early (E) clone frequency from h. h, Testes analyzed for presence and position of GFP negative clones at two, four, and ten DPHS. Clones were scored as Early (E) as outlined in a-c or Late (L) as in d if observed beyond the early mitotic amplification zone. Scale bars 20 µm. Supplemenatry Figure 3. Hub cells do not require shotgun for hub maintenance. a-e, Immunofluorescence images of 1-day old updgal4, UAS-gfp (a) or one (b) or twenty day old (c-e) updgal4, UAS-gfp; UAS-shgRNAi testes. a-a, The hub is labeled with DE-cadherin (DEC, red, a ) and GFP (green, a ) in updgal4, UAS-gfp testis. b-b, In updgal4, UAS-gfp; UAS-shgRNAi testes, DEC stain in the hub is lost (red, b ), but GFP labels the hub (green, b ). c-e, In twenty day old updgal4, UAS-gfp; UAS-shgRNAi testes, DEC stain in the hub is lost (red, c ), but GFP labels the hub (green, c, d, e ), FasIII labels the hub (red in d, d ), and TJ+ cells remain (red in e, e ). Scale bars 20 µm. 2
3 doi: /nature07173 SUPPLEMENTARY INFORMATION Supplementary Figure 4. SSC depletion by shotgun RNAi results in hub cell marker loss. a, c587gal4 drives expression of UAS-eGFP (green) in somatic cells (a ) but not in the FasII labeled hub (red, a ). Asterisk in a represents location of the hub. b, c, c587gal4>uas-shgrnai testes at 1-day (b) and 5-days (c) stained for FasIII (red, b, c ) and DE-cadherin (green, b, c ). FasIII expression is normal while DE-cadherin expression is significantly reduced with the hub (arrows). d-f, Control (d) and c587gal4>uas-shgrnai twenty-day old testes (e, f) stained for FasIII (red) and TJ (green). FasIII and TJ stain is reduced (e) or absent (f). g-i, Control (g) and c587gal4>uas-shgrnai 20-day old testes stained for DE-cadherin (red) and TJ (green). DE-cadherin and TJ stain is reduced (h) or absent (i). Scale bars 20 µm. 3
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8 doi: /nature07173 SUPPLEMENTARY INFORMATION Supplementary Table S1. SSC clonal analysis # Testes with labeled SSC at DPHS a Brief Genotype Heat shock protocol 1 DPHS 5 DPHS 10 DPHS 15 DPHS 30 DPHS tubulin-lacz 1 E1, E2 b 11/49 (22%) ND e ND ND ND 2 A1,A2 c 27/47 (57%) 21/74 (28%) 19/183 (10%) 23/225 (10%) 6/142 (4%) FRTG E1, E2 10/26 (38%) ND ND ND ND P9, P10 d 14/48 (29%) 13/78 (17%) 8/29 (28%) 4/49 (8%) ND FRTG13 shg IG E1, E2 0/5 (0%) ND ND ND ND P9, P10 11/38 (29%) 2/78 (3%) 0/53 (0%) 1/45 (2%) ND FRTG13 shg IH 4 2 E1, E2 0/14 (0%) ND ND ND ND P9, P10 7/59 (12%) 7/89 (8%) 1/49 (2%) 3/50 (6%) ND a Days Post Heat Shock (DPHS) b Embryos/early larvae were heat shocked for two hours on two consecutive days at days one and two after egg laying c Adult flies were collected and heat shocked for two hours on two consectutive at days one and two after eclosion d Late stage pupae were heat shocked for two hours on two consecutive days at days nine and ten after egg laying e No data 1 hsflp-12; X1529/X y,w, hsflp 122 ; FRTG13 α-tubulingal80/frtg13; 2x-UAS-eGFP/α-tubulinGAL4 3 y,w, hsflp 122 ; shg IG29 FRTG13 α-tubulingal80/frtg13; 2x-UAS-eGFP/α-tubulinGAL4 4 y,w, hsflp 122 ; shg IH FRTG13 α-tubulingal80/frtg13; 2x-UAS-eGFP/α-tubulinGAL4 8
9 Supplementary Table S2: Frequency of SSC contribution to the apical hub # Testes with labeled hub cells at DPHS a Genotype Heat shock protocol 1 DPHS 5 DPHS 10 DPHS 15 DPHS 30 DPHS tubulin-lacz 1 E1, E2 b 0/49 (0%) 16/47 A1, A2 c (34%) 35/74 (47%) 104/183 (57%) 136/225 (60%) no heat shock 0/52 (0%) 0/34 (0%) 0/19 (0%) 0/21 (0%) ND e Wild type 2 2 E1, E2 0/56 ND ND ND P9, P10 d (6%) (14%) 49/114 (35%) 72/110 (65%) 6/102 20/144 no heat shock 6/41 (15%) 4/38 (11%) 4/44 (9%) 0/6 (0%) FRT40A 3 2 E1, E2 0/30 (0%) ND ND ND P9, P10 d 6/54 (11%) 13/66 (19%) 41/85 (48%) 41/61 (67%) no heat shock 6/41 (15%) 1/7 (14%) 1/15 (7%) ND FRT40A esg G E1, E2 ND ND ND ND P9, P10 4/43 (9%) 4/43 (9%) 2/16 (13%) 8/27 (29%) no heat shcok ND 2/14 (14%) ND ND FRT40A esg L2 5 2 E1, E2 0/23 (0%) ND ND ND P9, P10 2/38 (5%) 1/40 (3%) 0/36 (0%) 2/52 (4%) no heat shock 0/25 (0%) 0/24 (0%) 0/5 (0%) 0/9 (0%) FRTG E1, E2 0/26 (0%) ND ND ND P9, P10 0/48 (0%) 7/78 (9%) 8/29 (28%) 31/49 (63%) no heat shock ND 3/31 (10%) 3/29 (10%) 0/6 (0%) FRTG13 shg IG E1, E2 0/5 (0%) ND ND ND P9, P10 4/38 (11%) 7/78 (9%) 18/53 (34%) 26/45 (58%) no heat shock ND 0/9 (0%) 1/6 (17%) ND FRTG13 shg IH 8 2 E1, E2 4/14 (29%) ND ND ND P9, P10 4/59 (7%) 4/89 (4%) 18/49 (37%) 25/50 (50%) no heat shock ND 3/25 (12%) 1/9 (11%) ND 88/142 (61%) a Days Post Heat Shock (DPHS) b Embryos/early larvae were heat shocked for two hours on two consecutive days at days one and two after egg laying c Adult flies were collected and heat shocked for two hours on two consectutive at days one and two after eclosion d Late stage pupae were heat shocked for two hours on two consecutive days at days nine and ten after egg laying e ND 1 hsflp-12; X1529/X Data pooled from FRT40A and FRTG13 3 y,w, hsflp 122 ; FRT40A α-tubulingal80/frt40a; 2x-UAS-eGFP/α-tubulinGAL4 4 y,w, hsflp 122 ; esg G66 FRT40A α-tubulingal80/frt40a; 2x-UAS-eGFP/α-tubulinGAL4 5 y,w, hsflp 122 ; esg L2 FRT40A α-tubulingal80/frt40a; 2x-UAS-eGFP/α-tubulinGAL4 6 y,w, hsflp 122 ; FRTG13 α-tubulingal80/frtg13; 2x-UAS-eGFP/α-tubulinGAL4 7 y,w, hsflp 122 ; shg IG29 FRTG13 α-tubulingal80/frtg13; 2x-UAS-eGFP/α-tubulinGAL4 8 y,w, hsflp 122 ; shg IH FRTG13 α-tubulingal80/frtg13; 2x-UAS-eGFP/α-tubulinGAL4 9
10 doi: /nature07173 SUPPLEMENTARY INFORMATION Supplementary Table S3: Frequency of BrdU and phh3 marked hub cells # Testes with BrdU+ Hub cells Genotype Pulse a 1 d chase 3 d chase 5 d chase 7-8 d chase 10d chase 15d chase Oregon R 1 d adult 0/82 (0%) ND b 6/143 (4%) 8/103 (8%) 3/96 (3%) 0/18 (0%) 5 d adult ND 2/52 (4%) ND ND ND ND 10 d adult ND 0/47 (0%) ND ND ND ND 15 d adult ND 1/57 (2%) ND ND ND ND Testes with phh3 marked hub cells Heat shock 1 DPHS 5 DPHS 10 DPHS 15 DPHS updgal4, UAS-gfp no heat shock 0/31 (0%) ND 0/31 (0%) ND 2 1d A c 0/128 (0%) 0/37 (0%) ND 0/57 (0%) a Flies allowed to feed upon 100mM BrdU dissolved in grape juice for 30 minutes b No data c Adult flies were collected and heat shocked for two hours at 37 o C 10
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a 0,8 Figure S1 8 h 12 h y = 0,036x + 0,2115 y = 0,0366x + 0,206 Labeling index Labeling index ctrl shrna Time (h) Time (h) ctrl shrna S G2 M G1
(GFP+ BrdU+)/GFP+ Labeling index Labeling index Figure S a, b, y =,x +, y =,x +,,,,,,,, Time (h) - - Time (h) c d S G M G h M G S G M G S G h Time of BrdU injection after electroporation (h) M G S G M
Contents. Research Articles
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SUPPLEMENTARY FIGURES 1 2 3 4 SUPPLEMENTARY TABLES Supplementary Table S1. Brain Tumors used in the study Code Tumor Classification Age Gender HuTuP51 Glioblastoma 57 Male HuTuP52 Glioblastoma 53 Male
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DOI: 10.1038/ncb3076 Supplementary Figure 1 btrcp targets Cep68 for degradation during mitosis. a) Cep68 immunofluorescence in interphase and metaphase. U-2OS cells were transfected with control sirna
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Supplementary Figure 1. Normal AMPAR-mediated fepsp input-output curve in CA3-Psen cdko mice. Input-output curves, which are plotted initial slopes of the evoked fepsp as function of the amplitude of the
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DOI: 10.1038/ncb2566 Figure S1 CDKL5 protein expression pattern and localization in mouse brain. (a) Multiple-tissue western blot from a postnatal day (P) 21 mouse probed with an antibody against CDKL5.
The subcortical maternal complex controls symmetric division of mouse zygotes by
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DOI: 10.1038/ncb2157 Figure S1 Immobilization of histone pre-mrna to chromatin leads to formation of histone locus body with associated Cajal body. Endogenous histone H2b(e) pre-mrna is processed with
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doi: 10.1038/nature06994 A phosphatase cascade by which rewarding stimuli control nucleosomal response A. Stipanovich*, E. Valjent*, M. Matamales*, A. Nishi, J.H. Ahn, M. Maroteaux, J. Bertran-Gonzalez,
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Supplementary Figures
J. Cell Sci. 128: doi:10.1242/jcs.173807: Supplementary Material Supplementary Figures Fig. S1 Fig. S1. Description and/or validation of reagents used. All panels show Drosophila tissues oriented with
Nature Neuroscience: doi: /nn Supplementary Figure 1. MADM labeling of thalamic clones.
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THE mechanisms that control maintenance of stem (Watt and Hogan 2000; Spradling et al. 2001). Discovery
Copyright 2004 by the Genetics Society of America DOI: 10.1534/genetics.103.023184 A Misexpression Screen Reveals Effects of bag-of-marbles and TGF Class Signaling on the Drosophila Male Germ-Line Stem
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