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大鼠睾丸中表达的电压门控钾通道的分子特征

Molecular characterization of a voltage-gated potassium channel expressed in rat testis.

作者信息

Jacob A, Hurley I R, Goodwin L O, Cooper G W, Benoff S

机构信息

Department of Obstetrics and Gynecology, North Shore University Hospital-New York University School of Medicine, Manhasset, New York 11030, USA.

出版信息

Mol Hum Reprod. 2000 Apr;6(4):303-13. doi: 10.1093/molehr/6.4.303.

Abstract

Potassium (K(+)) channels are present in both mammalian testis and spermatozoa. Immunofluorescent detection of sperm-bound biotinylated charybdotoxin, an inhibitor of Ca(2+)-activated and of delayed rectifier K(+) channels, indicated that these ion channels are uniformly distributed over the surface of both heads and tails of unfixed rat epididymal spermatozoa. Reverse transcription-polymerase chain reaction (RT-PCR) analysis on rat testis RNA with PCR primers, based on known nucleotide sequences of different classes of K(+) channels, amplified sequences homologous to delayed rectifier K(+) channels. In-situ RT-PCR on rat testis sections showed that these K(+) channel transcripts are present in the cytoplasm of primary spermatocytes and post-meiotic elongating spermatids. Northern blot analysis of various rat tissues identified multiple K(+) channel transcripts, some of which were observed only in testis. An attempt to obtain a full length rat testis K(+) channel cDNA sequence gave an assembled sequence of 2693 base pairs with >90% homology to a delayed rectifier K(+) channel, Kv1.3. A method for rapid amplification of cDNA ends was employed to amplify the 5' sequences of the rat testis cDNA but a unique sequence could not be obtained. DNA sequencer traces suggest that multiple related K(+) channels which differed at their 5' ends were amplified in rat testis.

摘要

钾离子(K(+))通道存在于哺乳动物的睾丸和精子中。用免疫荧光法检测与精子结合的生物素化蝎毒素(一种钙激活钾通道和延迟整流钾通道的抑制剂),结果表明这些离子通道均匀分布在未固定的大鼠附睾精子的头部和尾部表面。基于不同类型钾通道的已知核苷酸序列设计PCR引物,对大鼠睾丸RNA进行逆转录-聚合酶链反应(RT-PCR)分析,扩增出与延迟整流钾通道同源的序列。对大鼠睾丸切片进行原位RT-PCR显示,这些钾通道转录本存在于初级精母细胞和减数分裂后伸长的精子细胞的细胞质中。对大鼠各种组织进行Northern印迹分析,鉴定出多个钾通道转录本,其中一些仅在睾丸中观察到。尝试获得大鼠睾丸钾通道cDNA全长序列,得到一个2693个碱基对的组装序列,与延迟整流钾通道Kv1.3的同源性>90%。采用一种快速扩增cDNA末端的方法来扩增大鼠睾丸cDNA的5'序列,但未获得唯一序列。DNA测序仪图谱表明,在大鼠睾丸中扩增出了多个在5'末端不同但相关的钾通道。

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