GDSL esterase/lipases OsGELP34 and OsGELP110/OsGELP115 are e
發(fā)布時間:2021-10-15 06:00
Pollen exine contains complex biopolymers of aliphatic lipids and phenolics. Abnormal development of pollen exine often leads to plant sterility. Molecular mechanisms regulating exine formation have been studied extensively but remain ambiguous. Here we report the analyses of three GDSL esterase/lipase protein genes,OsGELP34, OsG ELP110, and Os GELP115, for rice exine formation. OsGELP34 was identified by cloning of a male sterile mutant gene. OsG ELP34 encodes an endoplasmic reticulum protein a...
【文章來源】:Journal of Integrative Plant Biology. 2020,62(10)SCICSCD
【文章頁數(shù)】:20 頁
【文章目錄】:
INTRODUCTIONO
RESULTS
Isolation and genetic analysis of the male sterile mutant osgelp34
Cloning of the mutant gene
The mutant gene encodes a putative GDSL lipase/esterase
Os GELP34 is mainly expressed in anthers during meiosis
Microscopic analysis of the mutant anther development
Mutation of Os GELP34 affected the expression of multiple genes acting in the tapetal PCD and pollen exine formation
Os GELP110 and Os GELP115 are redundant but essential for pollen development
DISCUSSION
MATERIALS AND METHODS
Plant materials and growth conditions
Characterization of the mutant phenotype
Microscopy and histology
Molecular cloning of Os GELP34 and HRM analysis
Plasmid construction,rice transformation,and transgene determination
Gene expression analysis by q RT‐PCR
GUS staining
Protein subcellular localization assay
Computational analysis of the GELP proteins
AUTHOR CONTRIBUTIONS
SUPPORTING INFORMATION
本文編號:3437554
【文章來源】:Journal of Integrative Plant Biology. 2020,62(10)SCICSCD
【文章頁數(shù)】:20 頁
【文章目錄】:
INTRODUCTIONO
RESULTS
Isolation and genetic analysis of the male sterile mutant osgelp34
Cloning of the mutant gene
The mutant gene encodes a putative GDSL lipase/esterase
Os GELP34 is mainly expressed in anthers during meiosis
Microscopic analysis of the mutant anther development
Mutation of Os GELP34 affected the expression of multiple genes acting in the tapetal PCD and pollen exine formation
Os GELP110 and Os GELP115 are redundant but essential for pollen development
DISCUSSION
MATERIALS AND METHODS
Plant materials and growth conditions
Characterization of the mutant phenotype
Microscopy and histology
Molecular cloning of Os GELP34 and HRM analysis
Plasmid construction,rice transformation,and transgene determination
Gene expression analysis by q RT‐PCR
GUS staining
Protein subcellular localization assay
Computational analysis of the GELP proteins
AUTHOR CONTRIBUTIONS
SUPPORTING INFORMATION
本文編號:3437554
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