2021
DOI: 10.1101/2021.01.13.426551
|View full text |Cite
Preprint
|
Sign up to set email alerts
|

Female gametophyte expressedArabidopsis thalianalipid transfer proteins AtLtpI.4 and AtLtpI.8 provide a link between callose homeostasis, pollen tube guidance, and fertilization success

Abstract: Non-specific lipid transfer proteins (LTPs) represent a sub-class among the large family of Cysteine-rich proteins (CRPs) specific to land plants. LTPs possess a hydrophobic cavity, enabling them to bind and stabilize a variety of lipid molecules outside membranes. In line with the existence of an N-terminal signal peptide, secreted LTPs represent a well-suited mobile signal carrier in the plant’s extracellular matrix. Thus, LTPs are currently considered as key players to mediate the bulk flow of lipids betwee… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2021
2021

Publication Types

Select...
1

Relationship

1
0

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 70 publications
(87 reference statements)
0
1
0
Order By: Relevance
“…To generate the MpBK2a::YFP construct, the full-length USER-PCR (described in `Cloning of the Marchantia BK channel gene’) was cloned into the binary vector pCAMBIA 2300 (35S:USER::YFP:35STerm) using the advanced uracil excision-based cloning technique [61, 62]. Agrobacterium tumefaciens cells of strain GV3101 were used for transformation and the preparation of the bacterial suspension is described in [65]. For transient transformation, Nicotiana benthamiana leaves of 3-week-old plants were infiltrated at their abaxial side with the bacterial suspension.…”
Section: Methodsmentioning
confidence: 99%
“…To generate the MpBK2a::YFP construct, the full-length USER-PCR (described in `Cloning of the Marchantia BK channel gene’) was cloned into the binary vector pCAMBIA 2300 (35S:USER::YFP:35STerm) using the advanced uracil excision-based cloning technique [61, 62]. Agrobacterium tumefaciens cells of strain GV3101 were used for transformation and the preparation of the bacterial suspension is described in [65]. For transient transformation, Nicotiana benthamiana leaves of 3-week-old plants were infiltrated at their abaxial side with the bacterial suspension.…”
Section: Methodsmentioning
confidence: 99%