1. Sertoli cell signaling by Desert hedgehog regulates the male germline
Mark J Bitgood, Liya Shen, Andrew P McMahon 
Current Biology 
Volume 6, Issue 3, Pages (March 1996)
DOI: /S (02)

2. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

3. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

4. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

5. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

6. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

7. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

8. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

9. Figure 1
Dhh expression in the gonad. (a–d) Expression in the 11.5 dpc urogenital ridge (ug). Transcripts were detected in the male (M), but not the female (F) gonad (a, aorta). (e,f) Expression in wild-type males (w.t.) and in males homozygous for the SlJ allele. Transcripts were detected in the Sertoli cell precursors of the germ-cell-deficient homozygote. (g)MIS expression in the 11.5 dpc male urogenital ridge. (h)Dhh expression in the adult testis. (a,b) Whole mount in situ hybridization performed with digoxygenin-labeled probes; (c–h) section in situ hybridization performed using 35S-labeled probes.
Current Biology 1996 6, DOI: ( /S (02) )

10. Figure 2
Homologous recombination at the Dhh locus. (a) Targeting construct. In the targeted allele, exons 1 and 2 and part of exon 3 of Dhh were replaced with the neomycin phosphotransferase selection cassette. (b) Hybridization of a Southern blot of EcoRI-digested wild-type, heterozygous and homozygous DNA with the 5′ probe shown in (a). The 26 kilobase (kb) band (corresponding to the wild-type gene) and the 24 kb band (corresponding to the mutant gene) were present as predicted. (c) Hybridization with a probe generated from exons 1 and 2. No band was detected in the homozygote. The loading control probe was from the Wnt-1 locus. B, BamHI; E, EcoRI; K, KpnI; N, NotI.
Current Biology 1996 6, DOI: ( /S (02) )

11. Figure 2
Homologous recombination at the Dhh locus. (a) Targeting construct. In the targeted allele, exons 1 and 2 and part of exon 3 of Dhh were replaced with the neomycin phosphotransferase selection cassette. (b) Hybridization of a Southern blot of EcoRI-digested wild-type, heterozygous and homozygous DNA with the 5′ probe shown in (a). The 26 kilobase (kb) band (corresponding to the wild-type gene) and the 24 kb band (corresponding to the mutant gene) were present as predicted. (c) Hybridization with a probe generated from exons 1 and 2. No band was detected in the homozygote. The loading control probe was from the Wnt-1 locus. B, BamHI; E, EcoRI; K, KpnI; N, NotI.
Current Biology 1996 6, DOI: ( /S (02) )

12. Figure 3
Testis development in Dhh mutants. (a,b) Urogenital systems of 18.5 dpc heterozygous and homozyogous males; (c,d) Urogenital systems of adult heterozygous and homozygous males (t, testis).
Current Biology 1996 6, DOI: ( /S (02) )

13. Figure 3
Testis development in Dhh mutants. (a,b) Urogenital systems of 18.5 dpc heterozygous and homozyogous males; (c,d) Urogenital systems of adult heterozygous and homozygous males (t, testis).
Current Biology 1996 6, DOI: ( /S (02) )

14. Figure 3
Testis development in Dhh mutants. (a,b) Urogenital systems of 18.5 dpc heterozygous and homozyogous males; (c,d) Urogenital systems of adult heterozygous and homozygous males (t, testis).
Current Biology 1996 6, DOI: ( /S (02) )

15. Figure 3
Testis development in Dhh mutants. (a,b) Urogenital systems of 18.5 dpc heterozygous and homozyogous males; (c,d) Urogenital systems of adult heterozygous and homozygous males (t, testis).
Current Biology 1996 6, DOI: ( /S (02) )

16. Figure 4
Comparison of post-partum heterozygous and homozygous testis mass. Bars represent average mass of both testes (TM) in an individual as a percentage of body mass (BM). Sample size appears within the bar; standard deviation is indicated.
Current Biology 1996 6, DOI: ( /S (02) )

17. Figure 5
Histological analysis of testis development in Dhh mutants. (a,b) Testicular tissue of heterozygous and homozygous adults (hemotoxylin and eosin stained). (c,d) Adult testicular tissue immunostained for the Sertoli-specific protein GATA-1. (e,f) Testicular tissue of 16 dpp heterozygous and homozygous mice (periodic acid–Schiff (PAS) stained).
Current Biology 1996 6, DOI: ( /S (02) )

18. Figure 5
Histological analysis of testis development in Dhh mutants. (a,b) Testicular tissue of heterozygous and homozygous adults (hemotoxylin and eosin stained). (c,d) Adult testicular tissue immunostained for the Sertoli-specific protein GATA-1. (e,f) Testicular tissue of 16 dpp heterozygous and homozygous mice (periodic acid–Schiff (PAS) stained).
Current Biology 1996 6, DOI: ( /S (02) )

19. Figure 5
Histological analysis of testis development in Dhh mutants. (a,b) Testicular tissue of heterozygous and homozygous adults (hemotoxylin and eosin stained). (c,d) Adult testicular tissue immunostained for the Sertoli-specific protein GATA-1. (e,f) Testicular tissue of 16 dpp heterozygous and homozygous mice (periodic acid–Schiff (PAS) stained).
Current Biology 1996 6, DOI: ( /S (02) )

20. Figure 5
Histological analysis of testis development in Dhh mutants. (a,b) Testicular tissue of heterozygous and homozygous adults (hemotoxylin and eosin stained). (c,d) Adult testicular tissue immunostained for the Sertoli-specific protein GATA-1. (e,f) Testicular tissue of 16 dpp heterozygous and homozygous mice (periodic acid–Schiff (PAS) stained).
Current Biology 1996 6, DOI: ( /S (02) )

21. Figure 5
Histological analysis of testis development in Dhh mutants. (a,b) Testicular tissue of heterozygous and homozygous adults (hemotoxylin and eosin stained). (c,d) Adult testicular tissue immunostained for the Sertoli-specific protein GATA-1. (e,f) Testicular tissue of 16 dpp heterozygous and homozygous mice (periodic acid–Schiff (PAS) stained).
Current Biology 1996 6, DOI: ( /S (02) )

22. Figure 5
Histological analysis of testis development in Dhh mutants. (a,b) Testicular tissue of heterozygous and homozygous adults (hemotoxylin and eosin stained). (c,d) Adult testicular tissue immunostained for the Sertoli-specific protein GATA-1. (e,f) Testicular tissue of 16 dpp heterozygous and homozygous mice (periodic acid–Schiff (PAS) stained).
Current Biology 1996 6, DOI: ( /S (02) )

23. Figure 6
Spermatogenesis in Dhh mutants. (a,b) Stage VI–VII seminiferous tubules in (a) heterozygous and (b) homozygous adults. Preleptotene (Pl) and pachytene (P) primary spermatocytes and spermatids at developmental steps 6–7 and 15 are present in both samples. (c) Stage VII–VIII seminiferous tubule of a heterozygous adult. Preleptotene–leptotene (L) and pachytene primary spermatocytes and spermatids at developmental steps 7–8 and 16 are visible. (d) Stage VII seminiferous tubule of a homozygote. Preleptotene–leptotene and pachytene primary spermatocytes and step 7 spermatids are observed; however, step 16 spermatids are absent. All samples were PAS stained.
Current Biology 1996 6, DOI: ( /S (02) )

24. Figure 6
Spermatogenesis in Dhh mutants. (a,b) Stage VI–VII seminiferous tubules in (a) heterozygous and (b) homozygous adults. Preleptotene (Pl) and pachytene (P) primary spermatocytes and spermatids at developmental steps 6–7 and 15 are present in both samples. (c) Stage VII–VIII seminiferous tubule of a heterozygous adult. Preleptotene–leptotene (L) and pachytene primary spermatocytes and spermatids at developmental steps 7–8 and 16 are visible. (d) Stage VII seminiferous tubule of a homozygote. Preleptotene–leptotene and pachytene primary spermatocytes and step 7 spermatids are observed; however, step 16 spermatids are absent. All samples were PAS stained.
Current Biology 1996 6, DOI: ( /S (02) )

25. Figure 6
Spermatogenesis in Dhh mutants. (a,b) Stage VI–VII seminiferous tubules in (a) heterozygous and (b) homozygous adults. Preleptotene (Pl) and pachytene (P) primary spermatocytes and spermatids at developmental steps 6–7 and 15 are present in both samples. (c) Stage VII–VIII seminiferous tubule of a heterozygous adult. Preleptotene–leptotene (L) and pachytene primary spermatocytes and spermatids at developmental steps 7–8 and 16 are visible. (d) Stage VII seminiferous tubule of a homozygote. Preleptotene–leptotene and pachytene primary spermatocytes and step 7 spermatids are observed; however, step 16 spermatids are absent. All samples were PAS stained.
Current Biology 1996 6, DOI: ( /S (02) )

26. Figure 6
Spermatogenesis in Dhh mutants. (a,b) Stage VI–VII seminiferous tubules in (a) heterozygous and (b) homozygous adults. Preleptotene (Pl) and pachytene (P) primary spermatocytes and spermatids at developmental steps 6–7 and 15 are present in both samples. (c) Stage VII–VIII seminiferous tubule of a heterozygous adult. Preleptotene–leptotene (L) and pachytene primary spermatocytes and spermatids at developmental steps 7–8 and 16 are visible. (d) Stage VII seminiferous tubule of a homozygote. Preleptotene–leptotene and pachytene primary spermatocytes and step 7 spermatids are observed; however, step 16 spermatids are absent. All samples were PAS stained.
Current Biology 1996 6, DOI: ( /S (02) )

27. Figure 7
Ptc expression in (a) heterozygous and (b) homozygous 18.5 dpc testis and epididymis. Ptctranscripts are detected in the peritubular Leydig cells in the testis (t) and in the mesenchyme of the epididymis (e) in the heterozygote. Only epididymal expression is observed in the homozygote.
Current Biology 1996 6, DOI: ( /S (02) )

28. Figure 7
Ptc expression in (a) heterozygous and (b) homozygous 18.5 dpc testis and epididymis. Ptctranscripts are detected in the peritubular Leydig cells in the testis (t) and in the mesenchyme of the epididymis (e) in the heterozygote. Only epididymal expression is observed in the homozygote.
Current Biology 1996 6, DOI: ( /S (02) )