Cargando…
The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants
In flowering plants, a haploid microspore undergoes an asymmetric division to produce the male germline that encounters a mitotic division to produce two germ cells. The resulting germ cells undergo a series of specialization events to produce the two sperm cells required for double fertilization. T...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099015/ https://www.ncbi.nlm.nih.gov/pubmed/35592143 http://dx.doi.org/10.1002/pld3.397 |
_version_ | 1784706509791297536 |
---|---|
author | Ali, Iftikhar Sher, Hassan Ullah, Zahid Ali, Ahmad Iqbal, Javed Yang, Wei‐Cai |
author_facet | Ali, Iftikhar Sher, Hassan Ullah, Zahid Ali, Ahmad Iqbal, Javed Yang, Wei‐Cai |
author_sort | Ali, Iftikhar |
collection | PubMed |
description | In flowering plants, a haploid microspore undergoes an asymmetric division to produce the male germline that encounters a mitotic division to produce two germ cells. The resulting germ cells undergo a series of specialization events to produce the two sperm cells required for double fertilization. These events include to upregulate male germline‐specific while downregulating male germline‐nonspecific regulon, but how these specializations events are regulated, are still unresolved. To know how plant sperm cell is specialized, we mutagenized Arabidopsis double homozygous transgenic line (MGH3p‐MGH3::eGFP and ACTIN11p‐H2B::mRFP) by an ethyl methane sulfonate (EMS) treatment and isolated a mutant with sperms identity loss, resulting in a completely male defective plant. Second‐generation sequencing identified a point mutation G/A causing premature stop codon TGG/TGA in the poly(A) polymerase PAPS1 that is linked with phenotype. Further, we found that paps1 mutant fails to upregulate male germline‐specific regulon and to downregulate male germline‐nonspecific factors required for sperm cell differentiation and attaining pollen maturation. Previously, polyadenylation of pre‐mRNAs by PAPS1 has been found crucial for both RNA‐based silencing processes and the processing of pre‐mRNAs into mature mRNAs ready for translation. This study concludes that PAPS1 mediates sperm cell differentiation through upregulating specific while silencing the nonspecific factors of male germlines. |
format | Online Article Text |
id | pubmed-9099015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90990152022-05-18 The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants Ali, Iftikhar Sher, Hassan Ullah, Zahid Ali, Ahmad Iqbal, Javed Yang, Wei‐Cai Plant Direct Original Research In flowering plants, a haploid microspore undergoes an asymmetric division to produce the male germline that encounters a mitotic division to produce two germ cells. The resulting germ cells undergo a series of specialization events to produce the two sperm cells required for double fertilization. These events include to upregulate male germline‐specific while downregulating male germline‐nonspecific regulon, but how these specializations events are regulated, are still unresolved. To know how plant sperm cell is specialized, we mutagenized Arabidopsis double homozygous transgenic line (MGH3p‐MGH3::eGFP and ACTIN11p‐H2B::mRFP) by an ethyl methane sulfonate (EMS) treatment and isolated a mutant with sperms identity loss, resulting in a completely male defective plant. Second‐generation sequencing identified a point mutation G/A causing premature stop codon TGG/TGA in the poly(A) polymerase PAPS1 that is linked with phenotype. Further, we found that paps1 mutant fails to upregulate male germline‐specific regulon and to downregulate male germline‐nonspecific factors required for sperm cell differentiation and attaining pollen maturation. Previously, polyadenylation of pre‐mRNAs by PAPS1 has been found crucial for both RNA‐based silencing processes and the processing of pre‐mRNAs into mature mRNAs ready for translation. This study concludes that PAPS1 mediates sperm cell differentiation through upregulating specific while silencing the nonspecific factors of male germlines. John Wiley and Sons Inc. 2022-05-12 /pmc/articles/PMC9099015/ /pubmed/35592143 http://dx.doi.org/10.1002/pld3.397 Text en © 2022 The Authors. Plant Direct published by American Society of Plant Biologists and the Society for Experimental Biology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Ali, Iftikhar Sher, Hassan Ullah, Zahid Ali, Ahmad Iqbal, Javed Yang, Wei‐Cai The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants |
title | The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants |
title_full | The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants |
title_fullStr | The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants |
title_full_unstemmed | The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants |
title_short | The poly(A) polymerase PAPS1 mediates pollen maturation by regulating sperm cell differentiation in plants |
title_sort | poly(a) polymerase paps1 mediates pollen maturation by regulating sperm cell differentiation in plants |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099015/ https://www.ncbi.nlm.nih.gov/pubmed/35592143 http://dx.doi.org/10.1002/pld3.397 |
work_keys_str_mv | AT aliiftikhar thepolyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT sherhassan thepolyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT ullahzahid thepolyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT aliahmad thepolyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT iqbaljaved thepolyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT yangweicai thepolyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT aliiftikhar polyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT sherhassan polyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT ullahzahid polyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT aliahmad polyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT iqbaljaved polyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants AT yangweicai polyapolymerasepaps1mediatespollenmaturationbyregulatingspermcelldifferentiationinplants |