#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

RAB-Like 2 Has an Essential Role in Male Fertility, Sperm Intra-Flagellar Transport, and Tail Assembly


A significant percentage of young men are infertile and, for the majority, the underlying cause remains unknown. Male infertility is, however, frequently associated with defective sperm motility, wherein the sperm tail is a modified flagella/cilia. Conversely, a greater understanding of essential mechanisms involved in tail formation may offer contraceptive opportunities, or more broadly, therapeutic strategies for global cilia defects. Here we have identified Rab-like 2 (RABL2) as an essential requirement for sperm tail assembly and function. RABL2 is a member of a poorly characterized clade of the RAS GTPase superfamily. RABL2 is highly enriched within developing male germ cells, where it localizes to the mid-piece of the sperm tail. Lesser amounts of Rabl2 mRNA were observed in other tissues containing motile cilia. Using a co-immunoprecipitation approach and RABL2 affinity columns followed by immunochemistry, we demonstrated that within developing haploid germ cells RABL2 interacts with intra-flagella transport (IFT) proteins and delivers a specific set of effector (cargo) proteins, including key members of the glycolytic pathway, to the sperm tail. RABL2 binding to effector proteins is regulated by GTP. Perturbed RABL2 function, as exemplified by the Mot mouse line that contains a mutation in a critical protein–protein interaction domain, results in male sterility characterized by reduced sperm output, and sperm with aberrant motility and short tails. Our data demonstrate a novel function for the RABL protein family, an essential role for RABL2 in male fertility and a previously uncharacterised mechanism for protein delivery to the flagellum.


Vyšlo v časopise: RAB-Like 2 Has an Essential Role in Male Fertility, Sperm Intra-Flagellar Transport, and Tail Assembly. PLoS Genet 8(10): e32767. doi:10.1371/journal.pgen.1002969
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002969

Souhrn

A significant percentage of young men are infertile and, for the majority, the underlying cause remains unknown. Male infertility is, however, frequently associated with defective sperm motility, wherein the sperm tail is a modified flagella/cilia. Conversely, a greater understanding of essential mechanisms involved in tail formation may offer contraceptive opportunities, or more broadly, therapeutic strategies for global cilia defects. Here we have identified Rab-like 2 (RABL2) as an essential requirement for sperm tail assembly and function. RABL2 is a member of a poorly characterized clade of the RAS GTPase superfamily. RABL2 is highly enriched within developing male germ cells, where it localizes to the mid-piece of the sperm tail. Lesser amounts of Rabl2 mRNA were observed in other tissues containing motile cilia. Using a co-immunoprecipitation approach and RABL2 affinity columns followed by immunochemistry, we demonstrated that within developing haploid germ cells RABL2 interacts with intra-flagella transport (IFT) proteins and delivers a specific set of effector (cargo) proteins, including key members of the glycolytic pathway, to the sperm tail. RABL2 binding to effector proteins is regulated by GTP. Perturbed RABL2 function, as exemplified by the Mot mouse line that contains a mutation in a critical protein–protein interaction domain, results in male sterility characterized by reduced sperm output, and sperm with aberrant motility and short tails. Our data demonstrate a novel function for the RABL protein family, an essential role for RABL2 in male fertility and a previously uncharacterised mechanism for protein delivery to the flagellum.


Zdroje

1. McLachlanRI, O'BryanMK (2010) Clinical Review#: State of the art for genetic testing of infertile men. J Clin Endocrinol Metab 95: 1013–1024.

2. de Kretser D.M LK, O'Bryan M.K. and Kerr J. (2006) The Cytology of the Testis and Intrinsic Control Mechanisms; Neil JD, editor. St. Louis, MO. USA: Elsevier Academic Press. 122 p.

3. KrisfalusiM, MikiK, MagyarPL, O'BrienDA (2006) Multiple glycolytic enzymes are tightly bound to the fibrous sheath of mouse spermatozoa. Biol Reprod 75: 270–278.

4. AfzeliusBA, EliassonR (1983) Male and female infertility problems in the immotile-cilia syndrome. Eur J Respir Dis Suppl 127: 144–147.

5. LeighMW, PittmanJE, CarsonJL, FerkolTW, DellSD, et al. (2009) Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genet Med 11: 473–487.

6. AdhiamboC, BlisnickT, ToutiraisG, DelannoyE, BastinP (2009) A novel function for the atypical small G protein Rab-like 5 in the assembly of the trypanosome flagellum. J Cell Sci 122: 834–841.

7. QinH, WangZ, DienerD, RosenbaumJ (2007) Intraflagellar transport protein 27 is a small G protein involved in cell-cycle control. Curr Biol 17: 193–202.

8. JamsaiD, O'BryanMK (2010) Genome-wide ENU mutagenesis for the discovery of novel male fertility regulators. Syst Biol Reprod Med 56: 246–259.

9. O'DonnellL, RhodesD, SmithSJ, MerrinerDJ, ClarkBJ, et al. (2012) An Essential Role for Katanin p80 and Microtubule Severing in Male Gamete Production. PLoS Genet 8: e1002698 doi:10.1371/journal.pgen.1002698.

10. BorgCL, WolskiKM, GibbsGM, O'BryanMK (2010) Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’. Hum Reprod Update 16: 205–224.

11. ColicelliJ (2004) Human RAS superfamily proteins and related GTPases. Sci STKE 2004: RE13.

12. AckersJP, DhirV, FieldMC (2005) A bioinformatic analysis of the RAB genes of Trypanosoma brucei. Mol Biochem Parasitol 141: 89–97.

13. Pereira-LealJB, SeabraMC (2000) The mammalian Rab family of small GTPases: definition of family and subfamily sequence motifs suggests a mechanism for functional specificity in the Ras superfamily. J Mol Biol 301: 1077–1087.

14. DiekmannY, SeixasE, GouwM, Tavares-CadeteF, SeabraMC, et al. (2011) Thousands of rab GTPases for the cell biologist. PLoS Comput Biol 7: e1002217 doi:10.1371/journal.pcbi.1002217.

15. SanyalAJ, Campbell-SargentC, MirshahiF, RizzoWB, ContosMJ, et al. (2001) Nonalcoholic steatohepatitis: association of insulin resistance and mitochondrial abnormalities. Gastroenterology 120: 1183–1192.

16. LuckerBF, BehalRH, QinH, SironLC, TaggartWD, et al. (2005) Characterization of the intraflagellar transport complex B core: direct interaction of the IFT81 and IFT74/72 subunits. J Biol Chem 280: 27688–27696.

17. WangZ, FanZC, WilliamsonSM, QinH (2009) Intraflagellar transport (IFT) protein IFT25 is a phosphoprotein component of IFT complex B and physically interacts with IFT27 in Chlamydomonas. PLoS ONE 4: e5384 doi:10.1371/journal.pone.0005384.

18. FollitJA, XuF, KeadyBT, PazourGJ (2009) Characterization of mouse IFT complex B. Cell Motil Cytoskeleton 66: 457–468.

19. WongAC, ShkolnyD, DormanA, WillinghamD, RoeBA, et al. (1999) Two novel human RAB genes with near identical sequence each map to a telomere-associated region: the subtelomeric region of 22q13.3 and the ancestral telomere band 2q13. Genomics 59: 326–334.

20. HutagalungAH, NovickPJ (2011) Role of Rab GTPases in membrane traffic and cell physiology. Physiol Rev 91: 119–149.

21. PaunescuTG, JonesAC, TyszkowskiR, BrownD (2008) V-ATPase expression in the mouse olfactory epithelium. Am J Physiol Cell Physiol 295: C923–930.

22. SchroderJM, LarsenJ, KomarovaY, AkhmanovaA, ThorsteinssonRI, et al. (2011) EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms. J Cell Sci 124: 2539–2551.

23. NakamuraN, MoriC, EddyEM (2010) Molecular complex of three testis-specific isozymes associated with the mouse sperm fibrous sheath: hexokinase 1, phosphofructokinase M, and glutathione S-transferase mu class 5. Biol Reprod 82: 504–515.

24. EddyEM (1999) Role of heat shock protein HSP70-2 in spermatogenesis. Rev Reprod 4: 23–30.

25. OdetF, DuanC, WillisWD, GouldingEH, KungA, et al. (2008) Expression of the gene for mouse lactate dehydrogenase C (Ldhc) is required for male fertility. Biol Reprod 79: 26–34.

26. SilvaDA, HuangX, BehalRH, ColeDG, QinH (2012) The RABL5 homolog IFT22 regulates the cellular pool size and the amount of IFT particles partitioned to the flagellar compartment in Chlamydomonas reinhardtii. Cytoskeleton (Hoboken) 69: 33–48.

27. OrtegaC, VerheyenG, RaickD, CamusM, DevroeyP, et al. (2011) Absolute asthenozoospermia and ICSI: what are the options? Hum Reprod Update 17: 684–692.

28. BadanoJL, MitsumaN, BealesPL, KatsanisN (2006) The ciliopathies: an emerging class of human genetic disorders. Annu Rev Genomics Hum Genet 7: 125–148.

29. Becker-HeckA, ZohnIE, OkabeN, PollockA, LenhartKB, et al. (2011) The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nat Genet 43: 79–84.

30. MerveilleAC, DavisEE, Becker-HeckA, LegendreM, AmiravI, et al. (2011) CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet 43: 72–78.

31. WilsonGR, WangHX, EganGF, RobinsonPJ, DelatyckiMB, et al. (2010) Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse. Hum Mol Genet 19: 1593–1602.

32. SironenA, KotajaN, MulhernH, WyattTA, SissonJH, et al. (2011) Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia. Biol Reprod 85: 690–701.

33. VoroninaVA, TakemaruK, TreutingP, LoveD, GrubbBR, et al. (2009) Inactivation of Chibby affects function of motile airway cilia. J Cell Biol 185: 225–233.

34. LeeL, CampagnaDR, PinkusJL, MulhernH, WyattTA, et al. (2008) Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1. Mol Cell Biol 28: 949–957.

35. FliegaufM, BenzingT, OmranH (2007) When cilia go bad: cilia defects and ciliopathies. Nat Rev Mol Cell Biol 8: 880–893.

36. CottonL, GibbsGM, Sanchez-PartidaLG, MorrisonJR, de KretserDM, et al. (2006) FGFR-1 [corrected] signaling is involved in spermiogenesis and sperm capacitation. J Cell Sci 119: 75–84.

37. GibbsGM, OrtaG, ReddyT, KoppersAJ, Martinez-LopezP, et al. (2011) Cysteine-rich secretory protein 4 is an inhibitor of transient receptor potential M8 with a role in establishing sperm function. Proc Natl Acad Sci U S A 108: 7034–7039.

38. ArsovT, SilvaDG, O'BryanMK, SainsburyA, LeeNJ, et al. (2006) Fat aussie–a new Alstrom syndrome mouse showing a critical role for ALMS1 in obesity, diabetes, and spermatogenesis. Mol Endocrinol 20: 1610–1622.

39. CancelloR, TordjmanJ, PoitouC, GuilhemG, BouillotJL, et al. (2006) Increased infiltration of macrophages in omental adipose tissue is associated with marked hepatic lesions in morbid human obesity. Diabetes 55: 1554–1561.

40. MarchesiniG, BriziM, Morselli-LabateAM, BianchiG, BugianesiE, et al. (1999) Association of nonalcoholic fatty liver disease with insulin resistance. Am J Med 107: 450–455.

41. XuH, BarnesGT, YangQ, TanG, YangD, et al. (2003) Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J Clin Invest 112: 1821–1830.

42. LivakKJ, SchmittgenTD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25: 402–408.

43. GibbsGM, ScanlonMJ, SwarbrickJ, CurtisS, GallantE, et al. (2006) The cysteine-rich secretory protein domain of Tpx-1 is related to ion channel toxins and regulates ryanodine receptor Ca2+ signaling. J Biol Chem 281: 4156–4163.

44. De MasiF, ChiarellaP, WilhelmH, MassimiM, BullardB, et al. (2005) High throughput production of mouse monoclonal antibodies using antigen microarrays. Proteomics 5: 4070–4081.

45. GibbsGM, LoJC, NixonB, JamsaiD, O'ConnorAE, et al. (2010) Glioma pathogenesis-related 1-like 1 is testis enriched, dynamically modified, and redistributed during male germ cell maturation and has a potential role in sperm-oocyte binding. Endocrinology 151: 2331–2342.

46. ChristoforidisS, ZerialM (2000) Purification and identification of novel Rab effectors using affinity chromatography. Methods 20: 403–410.

47. JamsaiD, RijalS, BiancoDM, O'ConnorAE, MerrinerDJ, et al. (2010) A novel protein, sperm head and tail associated protein (SHTAP), interacts with cysteine-rich secretory protein 2 (CRISP2) during spermatogenesis in the mouse. Biol Cell 102: 93–106.

48. SchoebelS, OesterlinLK, BlankenfeldtW, GoodyRS, ItzenA (2009) RabGDI displacement by DrrA from Legionella is a consequence of its guanine nucleotide exchange activity. Mol Cell 36: 1060–1072.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2012 Číslo 10
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#