The lncRNA male-specific abdominal plays a critical role in Drosophila accessory gland development and male fertility

Autor: Elodie Prince, Mariana F. Wolfner, Jessica L. Sitnik, Robert K. Maeda, Yohan Frei, François Karch, Dragan Gligorov
Jazyk: angličtina
Rok vydání: 2018
Předmět:
0301 basic medicine
Central Nervous System
Male
Cancer Research
Organogenesis
Oviposition
Cell morphology
Genome
Biochemistry
Nervous System
Animals
Genetically Modified

Sexual Behavior
Animal

0302 clinical medicine
Electrochemistry
Medicine and Health Sciences
Drosophila Proteins
Genetics (clinical)
Drosophila Melanogaster
Eukaryota
Animal Models
Non-coding RNA
Phenotype
Cell biology
Nucleic acids
Insects
Chemistry
Phenotypes
Experimental Organism Systems
Physical Sciences
Drosophila
Female
RNA
Long Noncoding

Drosophila melanogaster
Cellular Structures and Organelles
Anatomy
Research Article
Secondary Cells
lcsh:QH426-470
Arthropoda
Biology
Research and Analysis Methods
03 medical and health sciences
Model Organisms
microRNA
Genetics
Animals
Molecular Biology
Ecology
Evolution
Behavior and Systematics

Biology and life sciences
Organisms
Cell Biology
biology.organism_classification
Invertebrates
Gene regulation
Male accessory gland
lcsh:Genetics
MicroRNAs
030104 developmental biology
Electrochemical Cells
Fertility
Bithorax complex
Vacuoles
Mutation
Long non-coding RNAs
RNA
Gene expression
030217 neurology & neurosurgery
Zdroj: PLoS Genetics
PLoS Genetics, Vol 14, Iss 7, p e1007519 (2018)
ISSN: 1553-7404
1553-7390
Popis: Although thousands of long non-coding RNAs (lncRNA) have been identified in the genomes of higher eukaryotes, the precise function of most of them is still unclear. Here, we show that a >65 kb, male-specific, lncRNA, called male-specific abdominal (msa) is required for the development of the secondary cells of the Drosophila male accessory gland (AG). msa is transcribed from within the Drosophila bithorax complex and shares much of its sequence with another lncRNA, the iab-8 lncRNA, which is involved in the development of the central nervous system (CNS). Both lncRNAs perform much of their functions via a shared miRNA embedded within their sequences. Loss of msa, or of the miRNA it contains, causes defects in secondary cell morphology and reduces male fertility. Although both lncRNAs express the same miRNA, the phenotype in the secondary cells and the CNS seem to reflect misregulation of different targets in the two tissues.
Author summary In many animals, the male seminal fluid induces physiology changes in the mated female that increase a male’s reproductive success. These changes are often referred to as the post-mating response (PMR). In Drosophila, the seminal fluid proteins responsible for generating the PMR are made in a specialized gland, analogous to the mammalian seminal vesicle and prostate, called the accessory gland (AG). In this work, we show that a male-specific, long, non-coding RNA (lncRNA), called msa, plays a critical role in the development and function of this gland, primarily through a microRNA (miRNA) encoded within its sequence. This same miRNA had previously been shown to be expressed in the central nervous system (CNS) via an alternative promoter, where its ability to repress homeotic genes is required for both male and female fertility. Here, we present evidence that the targets of this miRNA in the AG are likely different from those found in the CNS. Thus, the same miRNA seems to have been selected to affect Drosophila fertility through two different mechanisms. Although many non-coding RNAs have now been identified, very few can be shown to have function. Our work highlights a lncRNA that has multiple biological functions, affecting cellular morphology and fertility.
Databáze: OpenAIRE
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