Stage-specific expression of proprotein form of hyaluronan binding protein 1 (HABP1) during spermatogenesis in rat

The presence of the 34‐kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al., 1994: Mol Reprod Dev 38:69–76). In the present communication, we examined the expression of HABP1 in adult rat testis during spermatogenesis. Int...

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Published inMolecular reproduction and development Vol. 62; no. 2; pp. 223 - 232
Main Authors Bharadwaj, Archana, Ghosh, Ilora, Sengupta, Aniruddha, Cooper, Trevor G., Weinbauer, Gerhard F., Brinkworth, Martin H., Nieschlag, Eberhard, Datta, Kasturi
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LanguageEnglish
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Abstract The presence of the 34‐kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al., 1994: Mol Reprod Dev 38:69–76). In the present communication, we examined the expression of HABP1 in adult rat testis during spermatogenesis. Interestingly, using anti‐rHABP1 antibody, we detected a protein of 55 kDa which was present only in testis, but not in other somatic tissues like spleen and liver. However, even in testis, only one transcript of HABP1 mRNA of 1.63 kb was observed. In addition, we confirm that this testis‐specific 55 kDa protein was immunologically identical with proprotein form of HABP1 using antibody raised against a decapeptide present in the proprotein region of HABP1. Comparative immunohistochemistry of testis, spleen, and liver tissues using both the antibodies supported the observation that the proprotein form of HABP1 is present only in testis. Higher mRNA expression of HABP1 in testis as compared to that of liver and spleen could be speculated from the RT‐PCR product. Finally, detailed study of the immunohistochemical staining of the seminiferous tubules revealed the expression of the HABP1 proprotein in specific stages of germ cells, like pachytene spermatocytes and round spermatids, but not in elongated ones, suggesting a possible role of HABP1 proprotein in spermatogenic differentiation. Mol. Reprod. Dev. 62: 223–232, 2002. © 2002 Wiley‐Liss, Inc.
AbstractList The presence of the 34‐kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al., 1994 : Mol Reprod Dev 38:69–76). In the present communication, we examined the expression of HABP1 in adult rat testis during spermatogenesis. Interestingly, using anti‐rHABP1 antibody, we detected a protein of 55 kDa which was present only in testis, but not in other somatic tissues like spleen and liver. However, even in testis, only one transcript of HABP1 mRNA of 1.63 kb was observed. In addition, we confirm that this testis‐specific 55 kDa protein was immunologically identical with proprotein form of HABP1 using antibody raised against a decapeptide present in the proprotein region of HABP1. Comparative immunohistochemistry of testis, spleen, and liver tissues using both the antibodies supported the observation that the proprotein form of HABP1 is present only in testis. Higher mRNA expression of HABP1 in testis as compared to that of liver and spleen could be speculated from the RT‐PCR product. Finally, detailed study of the immunohistochemical staining of the seminiferous tubules revealed the expression of the HABP1 proprotein in specific stages of germ cells, like pachytene spermatocytes and round spermatids, but not in elongated ones, suggesting a possible role of HABP1 proprotein in spermatogenic differentiation. Mol. Reprod. Dev. 62: 223–232, 2002. © 2002 Wiley‐Liss, Inc.
The presence of the 34-kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al., 1994: Mol Reprod Dev 38:69-76). In the present communication, we examined the expression of HABP1 in adult rat testis during spermatogenesis. Interestingly, using anti-rHABP1 antibody, we detected a protein of 55 kDa which was present only in testis, but not in other somatic tissues like spleen and liver. However, even in testis, only one transcript of HABP1 mRNA of 1.63 kb was observed. In addition, we confirm that this testis-specific 55 kDa protein was immunologically identical with proprotein form of HABP1 using antibody raised against a decapeptide present in the proprotein region of HABP1. Comparative immunohistochemistry of testis, spleen, and liver tissues using both the antibodies supported the observation that the proprotein form of HABP1 is present only in testis. Higher mRNA expression of HABP1 in testis as compared to that of liver and spleen could be speculated from the RT-PCR product. Finally, detailed study of the immunohistochemical staining of the seminiferous tubules revealed the expression of the HABP1 proprotein in specific stages of germ cells, like pachytene spermatocytes and round spermatids, but not in elongated ones, suggesting a possible role of HABP1 proprotein in spermatogenic differentiation.
The presence of the 34‐kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al., 1994: Mol Reprod Dev 38:69–76). In the present communication, we examined the expression of HABP1 in adult rat testis during spermatogenesis. Interestingly, using anti‐rHABP1 antibody, we detected a protein of 55 kDa which was present only in testis, but not in other somatic tissues like spleen and liver. However, even in testis, only one transcript of HABP1 mRNA of 1.63 kb was observed. In addition, we confirm that this testis‐specific 55 kDa protein was immunologically identical with proprotein form of HABP1 using antibody raised against a decapeptide present in the proprotein region of HABP1. Comparative immunohistochemistry of testis, spleen, and liver tissues using both the antibodies supported the observation that the proprotein form of HABP1 is present only in testis. Higher mRNA expression of HABP1 in testis as compared to that of liver and spleen could be speculated from the RT‐PCR product. Finally, detailed study of the immunohistochemical staining of the seminiferous tubules revealed the expression of the HABP1 proprotein in specific stages of germ cells, like pachytene spermatocytes and round spermatids, but not in elongated ones, suggesting a possible role of HABP1 proprotein in spermatogenic differentiation. Mol. Reprod. Dev. 62: 223–232, 2002. © 2002 Wiley‐Liss, Inc.
Author Cooper, Trevor G.
Weinbauer, Gerhard F.
Ghosh, Ilora
Nieschlag, Eberhard
Brinkworth, Martin H.
Bharadwaj, Archana
Sengupta, Aniruddha
Datta, Kasturi
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Issue 2
Keywords Spermatozoa
Rat
Spermatogenesis
Rodentia
Germinal cell
Cell differentiation
Gene expression
Testicle
Male genital system
Spermatid
Binding protein
Vertebrata
Mammalia
Spermatocyte
Language English
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Snippet The presence of the 34‐kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al.,...
The presence of the 34-kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al.,...
The presence of the 34‐kDa hyaluronan binding protein 1 (HABP1) on sperm surface and its role in fertilization is already established (Ranganathan et al., 1994...
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pascalfrancis
wiley
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SubjectTerms Animals
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Gene Expression
Hyaluronan Receptors - biosynthesis
Hyaluronan Receptors - genetics
hyaluronan-binding protein 1
Immunohistochemistry - methods
Male
Mammalian male genital system
Mitochondrial Proteins
Morphology. Physiology
proprotein form
Protein Precursors - biosynthesis
Protein Precursors - genetics
rat testis
Rats
Rats, Sprague-Dawley
Seminiferous Tubules - metabolism
sperm release
spermatogenesis
Spermatogenesis - physiology
Testis - growth & development
Testis - metabolism
Time Factors
Vertebrates: reproduction
Title Stage-specific expression of proprotein form of hyaluronan binding protein 1 (HABP1) during spermatogenesis in rat
URI https://api.istex.fr/ark:/67375/WNG-L76J43FP-P/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmrd.10135
https://www.ncbi.nlm.nih.gov/pubmed/11984833
https://search.proquest.com/docview/71719297
Volume 62
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