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Partial titin cDNA sequence isolated from rabbit cardiac muscle RNA.

作者信息

Fritz J D, Wolff J A, Greaser M L

机构信息

Department of Meat and Animal Science, University of Wisconsin-Madison 53706.

出版信息

J Muscle Res Cell Motil. 1993 Jun;14(3):347-50. doi: 10.1007/BF00123100.

DOI:10.1007/BF00123100
PMID:8360323
Abstract

Two regions of the rabbit cardiac titin cDNA were amplified from rabbit cardiac muscle total RNA using primers based on rabbit skeletal muscle titin (connectin) cDNAs. These 1.7 kb and 1.5 kb RNA-PCR products were based on the 3' regions of the skeletal muscle titin clones CE12 and MS2, respectively. The cDNA sequence of the 1.7 kb product was extended an additional 1.5 kb by a novel 3' extension technique which used random primers in RNA-PCR. The cardiac titin cDNAs were 99% identical in nucleotide sequence to their skeletal muscle counterparts and predicted two types of 100-residue repeats. Southern blot analysis suggested that both cardiac and skeletal titin are encoded by the same gene. PCR amplification of human genomic DNA with titin specific primers indicated that there is strong sequence similarity between rabbit and human titin sequences. The successful amplification of a 907 basepair region from human genomic DNA suggested that titin contains large exons which span multiple motif borders. This may be particularly advantageous in the processing of such a large RNA transcript.

摘要

相似文献

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2
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引用本文的文献

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J Muscle Res Cell Motil. 2001;22(2):149-62. doi: 10.1023/a:1010349416723.
2
Primary structure of the kinase domain region of rabbit skeletal and cardiac muscle titin.兔骨骼肌和心肌肌联蛋白激酶结构域区域的一级结构
J Muscle Res Cell Motil. 1996 Jun;17(3):343-8. doi: 10.1007/BF00240931.

本文引用的文献

1
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.杜兴氏肌营养不良症(DMD)cDNA的完整克隆以及正常个体和患病个体中DMD基因的初步基因组结构
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mRNA phenotyping by enzymatic amplification of randomly primed cDNA.通过随机引物cDNA的酶促扩增进行mRNA表型分析。
Nucleic Acids Res. 1988 Nov 11;16(21):10366. doi: 10.1093/nar/16.21.10366.
3
Sequence of an unusually large protein implicated in regulation of myosin activity in C. elegans.
与秀丽隐杆线虫肌球蛋白活性调节相关的一种异常大的蛋白质的序列。
Nature. 1989 Nov 2;342(6245):45-50. doi: 10.1038/342045a0.
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Quantitation of mRNA by the polymerase chain reaction.通过聚合酶链反应对mRNA进行定量分析。
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Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.使用热稳定DNA聚合酶进行引物引导的DNA酶促扩增。
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6
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.采用酸性硫氰酸胍-苯酚-氯仿萃取法一步分离RNA的方法。
Anal Biochem. 1987 Apr;162(1):156-9. doi: 10.1006/abio.1987.9999.
7
A regular pattern of two types of 100-residue motif in the sequence of titin.肌联蛋白序列中两种100个残基基序的规则模式。
Nature. 1990 May 17;345(6272):273-6. doi: 10.1038/345273a0.
8
A novel 3' extension technique using random primers in RNA-PCR.一种在RNA-PCR中使用随机引物的新型3'端延伸技术。
Nucleic Acids Res. 1991 Jul 11;19(13):3747. doi: 10.1093/nar/19.13.3747.
9
Towards a molecular understanding of titin.迈向对肌联蛋白的分子理解。
EMBO J. 1992 May;11(5):1711-6. doi: 10.1002/j.1460-2075.1992.tb05222.x.
10
Apolipoprotein B mRNA editing: a new tier for the control of gene expression.
Trends Biochem Sci. 1992 Feb;17(2):77-81. doi: 10.1016/0968-0004(92)90506-5.