scholarly journals Identification of TEX101 functional interactome through proteomic measurement of human spermatozoa homozygous for the missense variant rs35033974

2018 ◽  
Author(s):  
Christina Schiza ◽  
Dimitrios Korbakis ◽  
Keith Jarvi ◽  
Eleftherios P. Diamandis ◽  
Andrei P. Drabovich

SUMMARYTEX101 is a testis-specific cell-surface protein expressed exclusively in the male germ cells and a validated biomarker of male infertility. Mouse TEX101 was found essential for male fertility, and was suggested to function as a cell surface chaperone involved in maturation of proteins required for sperm migration and sperm-oocyte interaction. However, the precise functional role of human TEX101 is not known and cannot be studied in vitro due to the lack of human germ cell lines. Here, we genotyped 386 healthy fertile men and sub-fertile patients for a common and potentially deleterious missense variant rs35033974 of TEX101, and identified 52 heterozygous and 4 homozygous patients. We then discovered by targeted proteomics that the variant allele rs35033974 was associated with near-complete degradation (>97%) of the corresponding G99V TEX101 form, and suggested that spermatozoa of homozygous patients could serve as a knockdown model to study TEX101 function in humans. Differential proteomic profiling with label-free quantification measured 8,046 proteins in spermatozoa of eight men and identified 8 cell-surface and 9 secreted testis-specific proteins significantly down-regulated in four patients homozygous for rs35033974. Substantially reduced levels of testis-specific cell-surface proteins potentially involved in sperm migration and sperm-oocyte fusion (including LY6K and ADAM29) were confirmed by targeted proteomics and western blotting assays. Since recent population-scale genomic data revealed homozygous fathers with biological children, rs35033974 is not a single pathogenic factor of male infertility in humans. However, median TEX101 levels in seminal plasma were found 5-fold lower (P=0.0005) in heterozygous than in wild-type men of European ancestry. We conclude that spermatozoa of rs35033974 homozygous men have substantially reduced levels of TEX101 and could be used as a model to elucidate the precise TEX101 function, which will advance biology of human reproduction.Non-standard abbreviationsTEX101Testis-expressed sequence 101 proteinLY6KLymphocyte antigen 6 complex locus KADAM29A disintegrin and metalloproteinase domain-containing protein 29DPEP3Dipeptidase 3BH-adjusted t-testBenjamini-Hochberg-adjusted t-testFDRFalse discovery rateFWHMFull width at half maximumGPIGlycosylphosphatidylinositolLC-MS/MSliquid chromatography - tandem mass spectrometryLFQLabel-free quantificationMSMass spectrometrymAbMonoclonal antibodyMWUMann Whitney Unpaired t-testPRMParallel reaction monitoringROC AUCReceiver operating characteristic area under the curveSCXstrong cation exchange chromatographySPseminal plasmaSNVSingle nucleotide variationSRMSelected reaction monitoringWTwild-type

2018 ◽  
Author(s):  
Christina Schiza ◽  
Dimitrios Korbakis ◽  
Efstratia Panteleli ◽  
Keith Jarvi ◽  
Andrei P. Drabovich ◽  
...  

SUMMARYTEX101 is a testis-specific protein expressed exclusively in male germ cells and is a validated biomarker of male infertility. Studies in mice suggest that TEX101 is a cell-surface chaperone which regulates, through protein-protein interactions, the maturation of proteins involved in spermatozoa transit and oocyte binding. Male TEX101-null mice are sterile. Here, we identified by co-immunoprecipitation-mass spectrometry the interactome of human TEX101 in testicular tissues and spermatozoa. The testis-specific cell-surface dipeptidase 3 (DPEP3) emerged as the top hit. We further validated the TEX101-DPEP3 complex by using hybrid immunoassays. Combinations of antibodies recognizing different epitopes of TEX101 and DPEP3 facilitated development of a simple immunoassay to screen for disruptors of TEX101-DPEP3 complex. As a proof-of-a-concept, we demonstrated that anti-TEX101 antibody T4 disrupted the native TEX101-DPEP3 complex. Disrupting antibodies may be used to study the human TEX101-DPEP3 complex, and to develop modulators for male fertility.Non-standard abbreviationsTEX101Testis-expressed sequence 101 proteinDPEP3Dipeptidase 3AC-MSAffinity capture-mass spectrometryco-IP-MSCoimmunoprecipitation-mass spectrometryGPIGlycosylphosphatidylinositolLFQLabel-free quantificationmAbMonoclonal antibodyNHSN-hydroxysuccinimidePRMParallel reaction monitoringPTMPosttranslational modificationSPSeminal plasmaSRMSelected reaction monitoringFDRfalse detection rate


2007 ◽  
Vol 46 (22) ◽  
pp. 4180-4183 ◽  
Author(s):  
Hendrik Schroeder ◽  
Bernhard Ellinger ◽  
Christian F. W. Becker ◽  
Herbert Waldmann ◽  
Christof M. Niemeyer

2003 ◽  
Vol 92 (5) ◽  
pp. 234-241 ◽  
Author(s):  
D. James Morré ◽  
Dorothy M. Morré ◽  
Howard Sun ◽  
Raymond Cooper ◽  
Joseph Chang ◽  
...  

1984 ◽  
Vol 33 (2) ◽  
pp. 268-281 ◽  
Author(s):  
Ann M. Carroll ◽  
Michael Zalutsky ◽  
Sam Schatten ◽  
Atul Bhan ◽  
Linda L. Perry ◽  
...  

2010 ◽  
Vol 26 (6) ◽  
pp. 1544-1550
Author(s):  
Sandeep K. Arora ◽  
Rohit Sharma ◽  
Gagandeep Kaur ◽  
Preeti Bhoria ◽  
Maryada Sharma ◽  
...  

2018 ◽  
Vol 90 (10) ◽  
pp. 6131-6137 ◽  
Author(s):  
Baoyin Yuan ◽  
Yuanyuan Chen ◽  
Yuqiong Sun ◽  
Qiuping Guo ◽  
Jin Huang ◽  
...  

Development ◽  
1989 ◽  
Vol 105 (4) ◽  
pp. 795-802
Author(s):  
S.L. Goodman ◽  
R. Deutzmann ◽  
V. Nurcombe

The specific interaction of embryonal cells with the extracellular matrix (ECM) is one of the principal forces influencing embryonal development (Hay, 1984; Trinkaus, 1984). We used a muscle satellite cell line (MM14dy) to determine the relationship between locomotory response to laminin and the expression of specific cell surface binding sites for it. Time lapse videomicroscopic analysis was used to study the locomotory response and radioligand binding assays and cell attachment assays were used to follow the expression levels of binding sites for laminin and its subfragments E8 and E1–4. We report here the novel finding that the ability of MM14dy to locomote over laminin diminishes and finally vanishes as the cells differentiate. The simultaneous drop in expression of binding sites for laminin is interpreted as being of potential significance during development and repair.


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