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hsk1+是一种与酿酒酵母CDC7相关的粟酒裂殖酵母基因,是染色体复制所必需的。

hsk1+, a Schizosaccharomyces pombe gene related to Saccharomyces cerevisiae CDC7, is required for chromosomal replication.

作者信息

Masai H, Miyake T, Arai K

机构信息

Department of Molecular and Developmental Biology, University of Tokyo, Japan.

出版信息

EMBO J. 1995 Jul 3;14(13):3094-104. doi: 10.1002/j.1460-2075.1995.tb07312.x.

Abstract

Degenerate oligonucleotide-directed polymerase chain reaction was conducted to clone a possible Schizosaccharomyces pombe homologue [hsk1 for a putative homologue of CDC7 (seven) kinase 1] of Saccharomyces cerevisiae Cdc7 kinase. The cloned cDNA for hsk1+ contains an open reading frame consisting of 507 amino acids with predicted mol. wt of 58,370 that possesses overall amino acid identity of 46% (65% including similar residues) to CDC7. In addition to conserved domains for serine-threonine kinases, the predicted primary structure of Hsk1 contains three 'kinase insert' sequences characteristic to Cdc7 at the positions identical to those of Cdc7. Whereas the length and sequences of the kinase inserts are diverged between the two yeast species, 58% identity (76% including similar residues) is detected within the kinase conserved domains. The hsk1+ gene, which is present as a single copy on the S.pombe chromosome, contains two introns within the coding frame. Disruption of the hsk1+ gene by insertion of the ura4+ gene is lethal to growth. Analysis of the DNA content of germinating spores that contain hsk1 null alleles indicates that DNA replication is inhibited in the mutant. The morphology of these mutant spores after germination indicates abnormal nuclear division in some population of germinating spores, suggesting either that Hsk1 may be required for inhibition of mitosis until completion of S phase or that it may also be involved in proper execution of mitosis. Our results suggest that hsk1+ is a strong candidate for the functional fission yeast homologue of budding yeast CDC7 and that a mechanism through which initiation of chromosomal replication is regulated may be conserved between the two yeast species.

摘要

采用简并寡核苷酸定向聚合酶链反应克隆酿酒酵母Cdc7激酶可能的粟酒裂殖酵母同源物[假定的CDC7(七)激酶1的同源物hsk1]。克隆的hsk1⁺ cDNA包含一个由507个氨基酸组成的开放阅读框,预测分子量为58,370,与CDC7的整体氨基酸同一性为46%(包括相似残基在内为65%)。除了丝氨酸 - 苏氨酸激酶的保守结构域外,预测的Hsk1一级结构在与Cdc7相同的位置含有三个Cdc7特有的“激酶插入”序列。虽然两种酵母中激酶插入序列的长度和序列不同,但在激酶保守结构域内检测到58%的同一性(包括相似残基在内为76%)。hsk1⁺基因在粟酒裂殖酵母染色体上以单拷贝形式存在,在编码框内含有两个内含子。通过插入ura4⁺基因破坏hsk1⁺基因对生长是致死的。对含有hsk1无效等位基因的萌发孢子的DNA含量分析表明,突变体中DNA复制受到抑制。这些突变孢子萌发后的形态表明,在一些萌发孢子群体中核分裂异常,这表明Hsk1可能是抑制有丝分裂直至S期完成所必需的,或者它也可能参与有丝分裂的正常进行。我们的结果表明,hsk1⁺是芽殖酵母CDC7功能裂殖酵母同源物的有力候选者,并且两种酵母之间可能保守着一种调节染色体复制起始的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3018/394371/d7c600d8741e/emboj00037-0138-a.jpg

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