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首页> 外文期刊>Molecular biology of the cell >An InCytes from MBC Selection: Caenorhabditis elegans Teneurin, ten-1, Is Required for Gonadal and Pharyngeal Basement Membrane Integrity and Acts Redundantly with Integrin ina-1 and Dystroglycan dgn-1
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An InCytes from MBC Selection: Caenorhabditis elegans Teneurin, ten-1, Is Required for Gonadal and Pharyngeal Basement Membrane Integrity and Acts Redundantly with Integrin ina-1 and Dystroglycan dgn-1

机译:从MBC选择中获得的一种Inyyyte:秀丽隐杆线虫Teneurin,10-1,是性腺和咽部基底膜完整性所必需的,并与Integrin ina-1和Dystroglycan dgn-1冗余地起作用。

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摘要

The Caenorhabditis elegans teneurin ortholog, ten-1 , plays an important role in gonad and pharynx development. We found that lack of TEN-1 does not affect germline proliferation but leads to local basement membrane deficiency and early gonad disruption. Teneurin is expressed in the somatic precursor cells of the gonad that appear to be crucial for gonad epithelialization and basement membrane integrity. Ten-1 null mutants also arrest as L1 larvae with malformed pharynges and disorganized pharyngeal basement membranes. The pleiotropic phenotype of ten-1 mutant worms is similar to defects found in basement membrane receptor mutants ina-1 and dgn-1 as well as in the mutants of the extracellular matrix component laminin, epi-1 . We show that the ten-1 mutation is synthetic lethal with mutations of genes encoding basement membrane components and receptors due to pharyngeal or hypodermal defects. This indicates that TEN-1 could act redundantly with integrin INA-1, dystroglycan DGN-1, and laminin EPI-1 in C. elegans development. Moreover, ten-1 deletion sensitizes worms to loss of nidogen nid-1 causing a pharynx unattached phenotype in ten-1 ; nid-1 double mutants. We conclude that TEN-1 is important for basement membrane maintenance and/or adhesion in particular organs and affects the function of somatic gonad precursor cells.
机译:秀丽隐杆线虫teneurin ortholog 10-1在性腺和咽部发育中起重要作用。我们发现缺乏TEN-1不会影响种系增殖,但会导致局部基底膜缺乏和性腺早期分裂。 Teneurin在性腺的体细胞前体细胞中表达,这似乎对性腺上皮形成和基底膜完整性至关重要。 10-1个无效突变体也以L1幼虫的形式被捕,其咽部畸形且咽部基底膜紊乱。 10-1突变蠕虫的多效性表型类似于在基底膜受体突变体ina-1和dgn-1以及细胞外基质成分层粘连蛋白epi-1的突变体中发现的缺陷。我们表明,十-1突变是合成致死性的,由于咽或皮下缺损而导致的编码基膜成分和受体的基因突变。这表明TEN-1在秀丽隐杆线虫的发育中可能与整联蛋白INA-1,dystroglycan DGN-1和层粘连蛋白EPI-1重复作用。而且,ten-1缺失使蠕虫对nidogen nid-1的丢失敏感,从而导致ten-1中的咽部未附着表型。 nid-1双突变体。我们得出结论,TEN-1对于基底膜的维持和/或特定器官的粘附很重要,并影响体细胞性腺前体细胞的功能。

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