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Developmental program of PGK-1 and PGK-2 isozymes in spermatogenic cells of the mouse: Specific activities and rates of synthesis

机译:鼠标精子细胞中PGK-1和PGK-2同工酶的发育计划:特定的活性和合成率

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摘要

The specific activities and synthesis of the ubiquitous isozyme, PGK-1, and the testis-specific isozyme, PGK-2, have been quantitated and localized in spermatogenic cells of the mouse. There is a fivefold increase in total PGK specific activity between immature and adult testes which begins at approximately 30 days of age, coincident with the appearance of late-middle stage spermatids. The increase in total PGK is entirely due to the appearance and increase of the PGK-2 isozyme. Rates of PGK synthesis were measured by labeling testicular cells in vitro with [3H]leucine and purifying the PGK isozymes. When total testicular cells were examined, PGK-2 synthesis was detectable after 22 days of age at very low levels and increased in older testes to a level of 0.5% of total protein synthesis. PGK-1 synthesis remained relatively constant at all ages at a level 100-fold lower (0.005%). Testicular cells were separated into highly enriched fractions of particular spermatogenic stages by centrifugal elutriation. The PGK-1 synthesis rates were, again, very low and not significantly different between the various spermatogenic stages. PGK-2 synthesis was low to nondetectable in pachytene spermatocytes, increased to 0.07% in early spermatids and represented 0.7% of total protein synthesis in late spermatids. This increased rate of PGK-2 synthesis appears to require an increase in the amount of PGK-2 mRNA in late spermatids, cells in which no active RNA synthesis is detectable.
机译:普遍存在的同工酶,PGK-1和睾丸特异性同工酶PGK-2的具体活性和合成已经定量和定位在小鼠的精子细胞中。在未成熟和成年睾丸之间的PGK特异性活动总量的5倍增加,在大约30天的年龄开始,与后期半阶段的外观相一致。总PGK的增加完全是由于PGK-2同工酶的外观和增加。通过用[3H]亮氨酸在体外标记睾丸细胞并纯化PGK同工酶来测量PGK合成的速率。当检查总睾丸细胞时,PGK-2合成在非常低的水平下22天后可检测到,较旧的睾丸增加至总蛋白质合成的0.5%的水平。 PGK-1合成在所有年龄较低的所有年龄(0.005%)下保持相对恒定。通过离心次洗脱分离睾丸细胞分离成高度富集的特定精子源性阶段。 PGK-1合成率在各种精子发生阶段之间再次非常低,并且不会显着差异。 PGK-2合成低至樟脑精胶质细胞中不可选定,在早期精子中增加至0.07%,在后期精子中占总蛋白质合成的0.7%。这种增加的PGK-2合成率似乎需要在后期精子中的PGK-2 mRNA的量增加,其中没有可检测到活性RNA合成的细胞。

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